| 3. MANUFACTURING OPERATIONS - ACTIVE SUBSTANCES |
Active Substance:METHYLPREDNISOLONE |
|
3.1
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Manufacture of Active Substance by Chemical Synthesis
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| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
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| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
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3.5
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General Finishing Steps
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| 3.5.1 Physical processing steps: Drying, Micronization
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| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
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3.6
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Quality Control Testing
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| 3.6.1 Physical / Chemical testing |
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Active Substance:PARAMETHASONE ACETATE |
|
3.1
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Manufacture of Active Substance by Chemical Synthesis
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| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
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| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
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3.5
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General Finishing Steps
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| |
| 3.5.1 Physical processing steps: Drying
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| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
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3.6
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Quality Control Testing
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| 3.6.1 Physical / Chemical testing |
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Active Substance:CLOBETASOL PROPIONATE |
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3.1
|
Manufacture of Active Substance by Chemical Synthesis
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| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
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3.5
|
General Finishing Steps
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| 3.5.1 Physical processing steps: Drying, Micronization
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| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
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3.6
|
Quality Control Testing
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| |
| 3.6.1 Physical / Chemical testing |
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Active Substance:METHYLPREDNISOLONE ACETATE STERILE |
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3.1
|
Manufacture of Active Substance by Chemical Synthesis
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| 3.1.2 Manufacture of crude active substance Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
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| 3.1.3 Salt formation / Purification steps: Crystallization
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3.4
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Manufacture of sterile Active Substance
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| 3.4.1 Aseptically prepared |
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3.5
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General Finishing Steps
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| 3.5.1 Physical processing steps: Drying, Micronization
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| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
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3.6
|
Quality Control Testing
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| |
| 3.6.1 Physical / Chemical testing |
| 3.6.3 Microbiological testing including sterility testing |
| 3.6.4 Biological Testing |
|
Active Substance:TRIAMCINOLONE ACETONIDE STERILE |
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3.1
|
Manufacture of Active Substance by Chemical Synthesis
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| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
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3.4
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Manufacture of sterile Active Substance
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| 3.4.1 Aseptically prepared |
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3.5
|
General Finishing Steps
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| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
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3.6
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Quality Control Testing
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| |
| 3.6.1 Physical / Chemical testing |
| 3.6.3 Microbiological testing including sterility testing |
| 3.6.4 Biological Testing |
|
Active Substance:FLUNISOLIDE HEMIHYDRATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
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| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
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|
3.5
|
General Finishing Steps
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| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
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3.6
|
Quality Control Testing
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| |
| 3.6.1 Physical / Chemical testing |
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Active Substance:FLUOCINOLONE ACETONIDE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
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| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
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| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
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3.5
|
General Finishing Steps
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| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
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3.6
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Quality Control Testing
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| |
| 3.6.1 Physical / Chemical testing |
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Active Substance:BUSULFAN |
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3.1
|
Manufacture of Active Substance by Chemical Synthesis
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| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Highly toxic products
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| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
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3.5
|
General Finishing Steps
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| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
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3.6
|
Quality Control Testing
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| |
| 3.6.1 Physical / Chemical testing |
| 3.6.2 Microbiological testing excluding sterility testing |
| 3.6.4 Biological Testing |
|
Active Substance:FLUMETASONE PIVALATE |
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3.1
|
Manufacture of Active Substance by Chemical Synthesis
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| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
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|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
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3.6
|
Quality Control Testing
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| |
| 3.6.1 Physical / Chemical testing |
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Active Substance:HYDROCORTISONE ACETATE STERILE |
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3.1
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Manufacture of Active Substance by Chemical Synthesis
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| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
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|
3.4
|
Manufacture of sterile Active Substance
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| |
| 3.4.1 Aseptically prepared |
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|
3.5
|
General Finishing Steps
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| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
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3.6
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Quality Control Testing
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| |
| 3.6.1 Physical / Chemical testing |
| 3.6.3 Microbiological testing including sterility testing |
|
Active Substance:DIFLORASONE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
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| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
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3.6
|
Quality Control Testing
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| |
| 3.6.1 Physical / Chemical testing |
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Active Substance:CLOBETASONE BUTYRATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
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| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
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3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:CHLORMADINONE ACETATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
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| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
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|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
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3.6
|
Quality Control Testing
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| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:PREDNISOLONE SODIUM PHOSPHATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
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| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
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3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:TRIAMCINOLONE ACETONIDE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
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3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
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Active Substance:METHYLTESTOSTERONE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
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| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
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| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
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|
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3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
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3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:VAMOROLONE |
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3.1
|
Manufacture of Active Substance by Chemical Synthesis
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| |
| 3.1.1 Manufacture of active substance intermediates |
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
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|
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3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
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3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
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Active Substance:TRIAMCINOLONE HEXACETONIDE STERILE |
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3.1
|
Manufacture of Active Substance by Chemical Synthesis
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| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
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Quality Control Testing
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| |
| 3.6.1 Physical / Chemical testing |
| 3.6.3 Microbiological testing including sterility testing |
| 3.6.4 Biological Testing |
|
Active Substance:DESONIDE DISODIUM PHOSPHATE |
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3.1
|
Manufacture of Active Substance by Chemical Synthesis
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| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
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3.6
|
Quality Control Testing
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| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:PREDNISOLONE-21-HEXANOATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:METHYLPREDNISOLONE HYDROGEN SUCCINATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
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| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:MELPHALAN HYDROCHLORIDE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Highly toxic products
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
| 3.6.2 Microbiological testing excluding sterility testing |
| 3.6.4 Biological Testing |
|
Active Substance:TESTOSTERONE CYPIONATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:TRIAMCINOLONE DIACETATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:HYDROCORTISONE ACETATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:FLUDROCORTISONE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:MEDROGESTONE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:DIFLUCORTOLONE VALERATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:BUDESONIDE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:FLUMETASONE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:DESOXIMETASONE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:BECLOMETASONE DIPROPIONATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Purification
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:CYSTEAMINE BITARTRATE MONOHYDRATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates |
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
| 3.6.2 Microbiological testing excluding sterility testing |
|
Active Substance:TRIAMCINOLONE HEXACETONIDE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:FLUPREDNIDENE ACETATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:BUDESONIDE STERILE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.4
|
Manufacture of sterile Active Substance
|
| |
| 3.4.1 Aseptically prepared |
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:BETAMETHASONE VALERATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:MOMETASONE FUROATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:DEXAMETHASONE STERILE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.4
|
Manufacture of sterile Active Substance
|
| |
| 3.4.1 Aseptically prepared |
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
| 3.6.3 Microbiological testing including sterility testing |
|
Active Substance:MEDROXYPROGESTERONE ACETATE STERILE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
| 3.6.3 Microbiological testing including sterility testing |
| 3.6.4 Biological Testing |
|
Active Substance:CYPROTERONE ACETATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:DEXAMETHASONE SODIUM PHOSPHATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:FLUOCORTOLONE CAPROATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates |
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:FLUOROMETHOLONE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
| 3.6.2 Microbiological testing excluding sterility testing |
|
Active Substance:DIFLORASONE DIACETATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
| 3.6.2 Microbiological testing excluding sterility testing |
|
Active Substance:FULVESTRANT |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Purification
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
| 3.6.2 Microbiological testing excluding sterility testing |
|
Active Substance:BECLOMETASONE DIPROPIONATE STERILE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.4
|
Manufacture of sterile Active Substance
|
| |
| 3.4.1 Aseptically prepared |
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
| 3.6.3 Microbiological testing including sterility testing |
|
Active Substance:MEGESTROL ACETATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:DELMADINONE ACETATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:AMCINONIDE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:FLUNISOLIDE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:CANNABIDIOL (SYNTHETIC) |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates |
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:CANNABIDIOL (BY EXTRACTION) |
|
3.2
|
Extraction of Active Substance from Natural Sources
|
| |
| 3.2.1 Extraction of substance from plant source |
| 3.2.5 Modification of extracted substance Plant |
| 3.2.6 Purification of extracted substance Plant |
| 3.2.7 Other: Cannabis sativa L. apical parts with inflorescences
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
| 3.6.2 Microbiological testing excluding sterility testing |
|
Active Substance:DIFLUPREDNATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:BETAMETHASONE DIPROPIONATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
| 3.6.4 Biological Testing |
|
Active Substance:URSODEOXYCHOLIC ACID |
|
3.2
|
Extraction of Active Substance from Natural Sources
|
| |
| 3.2.5 Modification of extracted substance Animal |
| 3.2.6 Purification of extracted substance Animal |
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
| 3.6.2 Microbiological testing excluding sterility testing |
|
Active Substance:PREDNISOLONE ACETATE STERILE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.4
|
Manufacture of sterile Active Substance
|
| |
| 3.4.1 Aseptically prepared |
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
| 3.6.3 Microbiological testing including sterility testing |
|
Active Substance:HALOMETASONE MONOHYDRATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:HYDROCORTISONE HYDROGEN SUCCINATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:FORMOTEROL FUMARATE DIHYDRATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates |
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:FLUOCORTOLONE PIVALATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates |
| 3.1.2 Manufacture of crude active substance Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
| 3.6.2 Microbiological testing excluding sterility testing |
|
Active Substance:BREXANOLONE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:TIROFIBAN HYDROCHLORIDE MONOHYDRATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates |
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
| 3.6.2 Microbiological testing excluding sterility testing |
| 3.6.4 Biological Testing |
|
Active Substance:FLUOCINONIDE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:FLUDROXYCORTIDE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:PREDNISOLONE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:PREDNISOLONE 17-VALERATE 21-ACETATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:HALCINONIDE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:SALMETEROL XINAFOATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates |
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
| 3.6.2 Microbiological testing excluding sterility testing |
|
Active Substance:FLUTICASONE PROPIONATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:PREDNISOLONE ACETATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:PREDNISOLONE METASULFOBENZOATE SODIUM |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
| 3.6.2 Microbiological testing excluding sterility testing |
|
Active Substance:LOTEPREDNOL ETABONATE STERILE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.4
|
Manufacture of sterile Active Substance
|
| |
| 3.4.1 Aseptically prepared |
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
| 3.6.3 Microbiological testing including sterility testing |
|
Active Substance:EXEMESTANE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:NORURSODEOXYCHOLIC ACID |
|
3.2
|
Extraction of Active Substance from Natural Sources
|
| |
| 3.2.5 Modification of extracted substance Animal |
| 3.2.6 Purification of extracted substance Animal |
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
| 3.6.2 Microbiological testing excluding sterility testing |
|
Active Substance:DEXAMETHASONE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.2 Manufacture of crude active substance Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
| 3.6.2 Microbiological testing excluding sterility testing |
|
Active Substance:BECLOMETASONE DIPROPIONATE MONOHYDRATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:TRIAMCINOLONE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:CLOCORTOLONE PIVALATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:MIVACURIUM CHLORIDE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates |
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
| 3.6.2 Microbiological testing excluding sterility testing |
| 3.6.4 Biological Testing |
|
Active Substance:OSATERONE ACETATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:FLUDROCORTISONE ACETATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:DESONIDE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:LOTEPREDNOL ETABONATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:PREDNICARBATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:FLUTICASONE FUROATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
| 3.6.2 Microbiological testing excluding sterility testing |
|
Active Substance:METHYLPREDNISOLONE ACEPONATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
Active Substance:MEDROXYPROGESTERONE ACETATE |
|
3.1
|
Manufacture of Active Substance by Chemical Synthesis
|
| |
| 3.1.1 Manufacture of active substance intermediates Special Requirements: 7.Other: Other: Hormones or substances with hormonal activity
|
| 3.1.2 Manufacture of crude active substance |
| 3.1.3 Salt formation / Purification steps: Crystallization
|
|
|
3.5
|
General Finishing Steps
|
| |
| 3.5.1 Physical processing steps: Drying, Micronization
|
| 3.5.2 Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance) |
| 3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance) |
|
|
3.6
|
Quality Control Testing
|
| |
| 3.6.1 Physical / Chemical testing |
|
4. Other Activities - Active Substances:
Importation of: PREDNISOLONE (confidential), HYDROCORTISONE (confidential), METHYLPREDNISOLONE (confidential), PREGNENOLONE (confidential), TESTOSTERONE (confidential), CHOLIC ACID (confidential), BETAMETHASONE (confidential), BETAMETHASONE ACETATE (confidential), L-TYROSINE (confidential)