Eudra GMP - Public Layout

MIA | GMP | API REG | WDA | GDP | Sites

Help

Tue 10 Nov 2026 23:16:13 BST

GMP Compliance Menu

GMP Certificates

Non-Compliance Report

Print Preview

Print Preview (Short version)

Back To Search

Italian Medicines Agency

CERTIFICATE NUMBER: IT-API/275/H/2023

CERTIFICATE OF GMP COMPLIANCE OF A MANUFACTURER(1) , (2)

Part 1

Issued following an inspection in accordance with
Art. 111(5) of Directive 2001/83/EC as amended

The competent authority of Italy confirms the following:

The manufacturer: Farmabios S.p.A.

Site address:

Via Pavia 1, Gropello Cairoli, 27027, Italy

OMS Organisation Id. / OMS Location Id.: ORG-100011643 / LOC-100021232

Is an active substance manufacturer that has been inspected in accordance with Art. 111(1) of Directive 2001/83/EC0.

From the knowledge gained during inspection of this manufacturer, the latest of which was conducted on 2023-03-03 , it is considered that it complies with:

The principles of GMP for active substances referred to in Article 47 of Directive 2001/83/EC and an appropriate level of GMP as referred to in Article 46(f) of Directive 2001/83/EC.

This certificate reflects the status of the manufacturing site at the time of the inspection noted above and should not be relied upon to reflect the compliance status if more than three years have elapsed since the date of that inspection. However, this period of validity may be reduced or extended using regulatory risk management principles by an entry in the Restrictions or Clarifying remarks field. Updates to restrictions or clarifying remarks can be identified through the EudraGMDP website (https://eudragmdp.ema.europa.eu/). This certificate is valid only when presented with all pages and both Parts 1 and 2.

The authenticity of this certificate may be verified in EudraGMDP. If it does not appear, please contact the issuing authority.

__________________________________________________________________________________________________________________________

(1) The certificate referred to in paragraph Art. 111(5) of Directive 2001/83/ECis also applicable to importers.
(2) Guidance on the interpretation of this template can be found in the Interpretation of the Union format for GMP certificate.
(3) These requirements fulfil the GMP recommendations of WHO.

Part 2

Human Medicinal Products

Manufacture of active substance. Names of substances subject to inspection:

[00000000001223]DEXAMETHASONE(en)

[00000000001264]DESOXIMETASONE(en)

[00000000005888]TRIAMCINOLONE BENETONIDE(en)

[00000000003855]TRIAMCINOLONE DIACETATE(en)

[00000000002506]MELPHALAN HYDROCHLORIDE(en)

[00000000005327]FLUMETASONE(en)

[00000000005646]TRIAMCINOLONE ESACETONIDE(en)

[00000000001256]DESONIDE(en)

[0000000000568]BETAMETHASONE DIPROPIONATE(en)

[00000000001641]EXEMESTANE(en)

[00000000004264]FLUDROCORTISONE ACETATE(en)

[00000000002144]HYDROCORTISONE ACETATE(en)

[00000000007413]PREDNISOLONE ACETATE STERILE(en)

[00000000004228]DIFLUPREDNATE(en)

[00000000001821]FLUNISOLIDE(en)

[00000000001850]FLUOROMETHOLONE(en)

[00000000002725]MOMETASONE FUROATE(en)

[00000000002542]MEGESTROL ACETATE(en)

[00000000002645]METHYLTESTOSTERONE(en)

[00000000003211]PREDNISOLONE ACETATE(en)

[00000000003217]PREDNISOLONE 17-VALERATE 21-ACETATE(en)

[00000000001021]CLOBETASONE BUTYRATE(en)

[0000000000215]HALCINONIDE(en)

[00000000006004]BECLOMETASONE DIPROPIONATE MONOHYDRATE(en)

[00000000006005]CLOCORTOLONE PIVALATE(en)

[00000000009337]PREDNISOLONE-21-HEXANOATE(en)

[00000000001345]DIFLORASONE DIACETATE(en)

[0000000000285]HALOMETASONE MONOHYDRATE(en)

[0000000000307]AMCINONIDE(en)

[0000000000665]BUDESONIDE(en)

[00000000004268]FLUPREDNIDENE ACETATE(en)

[00000000001822]FLUNISOLIDE HEMIHYDRATE(en)

[00000000001948]FULVESTRANT(en)

[00000000003208]PREDNICARBATE(en)

[00000000003798]TIROFIBAN HYDROCHLORIDE MONOHYDRATE(en)

[00000000005452]HYDROCORTISONE ACETATE STERILE(en)

[00000000008722]CANNABIDIOL (BY EXTRACTION)(en)

[0000000000565]BETAMETHASONE VALERATE(en)

[00000000004207]CHLORMADINONE ACETATE(en)

[00000000004219]DELMADINONE ACETATE(en)

[00000000004263]FLUDROCORTISONE(en)

[00000000004337]OSATERONE ACETATE(en)

[00000000001812]FLUMETASONE PIVALATE(en)

[00000000001834]FLUOCINONIDE(en)

[00000000001880]FLUTICASONE FUROATE(en)

[00000000005588]PREDNISOLONE METASULFOBENZOATE SODIUM(en)

[00000000002151]HYDROCORTISONE HYDROGEN SUCCINATE(en)

[00000000002536]MEDROXYPROGESTERONE ACETATE(en)

[00000000002633]METHYLPREDNISOLONE ACEPONATE(en)

[0000000000165]URSODEOXYCHOLIC ACID(en)

[0000000000100861]TRIAMCINOLONE HEXACETONIDE STERILE(en)

[00000000004916]FLUDROXYCORTIDE(en)

[00000000001825]FLUOCINOLONE ACETONIDE(en)

[00000000001879]FLUTICASONE PROPIONATE(en)

[00000000001895]FORMOTEROL FUMARATE DIHYDRATE(en)

[00000000003853]TRIAMCINOLONE(en)

[00000000006159]TRIAMCINOLONE ACETONIDE STERILE(en)

[00000000007231]METHYLPREDNISOLONE ACETATE STERILE(en)

[00000000007688]ISOPROTERENOL HYDROCHLORIDE(en)

[00000000007962]NORURSODEOXYCHOLIC ACID(en)

[00000000007237]PARAMETHASONE ACETATE(en)

[00000000001347]DIFLUCORTOLONE VALERATE(en)

[0000000000688]BUSULFAN(en)

[00000000003444]SALMETEROL XINAFOATE(en)

[00000000001020]CLOBETASOL PROPIONATE(en)

[00000000005209]BECLOMETASONE DIPROPIONATE(en)

[00000000001259]DESONIDE DISODIUM PHOSPHATE(en)

[00000000002716]MIVACURIUM CHLORIDE(en)

[00000000002484]LOTEPREDNOL ETABONATE(en)

[00000000002630]METHYLPREDNISOLONE(en)

[00000000003854]TRIAMCINOLONE ACETONIDE(en)

[0000000000986]CYPROTERONE ACETATE(en)

[00000000005969]DIFLORASONE(en)

[00000000006157]MEDROXYPROGESTERONE ACETATE STERILE(en)

[00000000006158]BECLOMETASONE DIPROPIONATE STERILE(en)

[00000000007230]BUDESONIDE STERILE(en)

[00000000007192]CANNABIDIOL (SYNTHETIC)(en)

[00000000007232]LOTEPREDNOL ETABONATE STERILE(en)

[00000000008133]CYSTEAMINE BITARTRATE MONOHYDRATE(en)

3. MANUFACTURING OPERATIONS - ACTIVE SUBSTANCES

Active Substance:DEXAMETHASONE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
crystallisation

3.1.2  Manufacture of crude active substance
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.6 Quality Control Testing

3.6.2  Microbiological testing excluding sterility testing

3.6.1  Physical / Chemical testing

Active Substance:DESOXIMETASONE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:TRIAMCINOLONE BENETONIDE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
crystallisation

3.1.2  Manufacture of crude active substance

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the 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

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:MELPHALAN HYDROCHLORIDE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Cytotoxic

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.4  Biological Testing

3.6.2  Microbiological testing excluding sterility testing

3.6.1  Physical / Chemical testing

Active Substance:FLUMETASONE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
crystallisation

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:TRIAMCINOLONE ESACETONIDE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:DESONIDE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying,micronisation

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:
crystallisation

Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying,micronisation

3.6 Quality Control Testing

3.6.4  Biological Testing

3.6.1  Physical / Chemical testing

Active Substance:EXEMESTANE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:FLUDROCORTISONE ACETATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

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:
crystallisation

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:PREDNISOLONE ACETATE STERILE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
crystallisation

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.4 Manufacture of sterile Active Substance

3.4.1  Aseptically prepared

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying,micronisation

3.6 Quality Control Testing

3.6.3  Microbiological testing including sterility testing

3.6.1  Physical / Chemical testing

Active Substance:DIFLUPREDNATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:FLUNISOLIDE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:FLUOROMETHOLONE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
crystallisation

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.6 Quality Control Testing

3.6.2  Microbiological testing excluding sterility testing

3.6.1  Physical / Chemical testing

Active Substance:MOMETASONE FUROATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:MEGESTROL ACETATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying,micronisation

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:METHYLTESTOSTERONE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:PREDNISOLONE ACETATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
crystallisation

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the 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

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:CLOBETASONE BUTYRATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:HALCINONIDE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:BECLOMETASONE DIPROPIONATE MONOHYDRATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:CLOCORTOLONE PIVALATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:PREDNISOLONE-21-HEXANOATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
crystallisation

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:DIFLORASONE DIACETATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.2  Microbiological testing excluding sterility testing

3.6.1  Physical / Chemical testing

Active Substance:HALOMETASONE MONOHYDRATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:AMCINONIDE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:BUDESONIDE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:FLUPREDNIDENE ACETATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
crystallisation

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:FLUNISOLIDE HEMIHYDRATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:FULVESTRANT

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
purification

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.6 Quality Control Testing

3.6.2  Microbiological testing excluding sterility testing

3.6.1  Physical / Chemical testing

Active Substance:PREDNICARBATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

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

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.4  Biological Testing

3.6.2  Microbiological testing excluding sterility testing

3.6.1  Physical / Chemical testing

Active Substance:HYDROCORTISONE ACETATE STERILE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
crystallisation

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.4 Manufacture of sterile Active Substance

3.4.1  Aseptically prepared

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying,micronisation

3.6 Quality Control Testing

3.6.3  Microbiological testing including sterility testing

3.6.1  Physical / Chemical testing

Active Substance:CANNABIDIOL (BY EXTRACTION)

3.2 Extraction of Active Substance from Natural Sources

3.2.6  Purification of extracted substance Plant

3.2.5  Modification of extracted substance Plant

3.2.1  Extraction of substance from plant source

3.2.7  Other:
Cannabis sativa L, apical parts with inflorescences

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying

3.5.3  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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.6 Quality Control Testing

3.6.2  Microbiological testing excluding sterility 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:
crystallisation

Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying,micronisation

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:CHLORMADINONE ACETATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying,micronisation

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:DELMADINONE ACETATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:FLUDROCORTISONE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:OSATERONE ACETATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:FLUMETASONE PIVALATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:FLUOCINONIDE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying,micronisation

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:FLUTICASONE FUROATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
crystallisation

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.6 Quality Control Testing

3.6.2  Microbiological testing excluding sterility testing

3.6.1  Physical / Chemical testing

Active Substance:PREDNISOLONE METASULFOBENZOATE SODIUM

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
crystallisation

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.6 Quality Control Testing

3.6.2  Microbiological testing excluding sterility 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:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:MEDROXYPROGESTERONE ACETATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying,micronisation

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:METHYLPREDNISOLONE ACEPONATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
crystallisation

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying,micronisation

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:URSODEOXYCHOLIC ACID

3.2 Extraction of Active Substance from Natural Sources

3.2.6  Purification of extracted substance Animal

3.2.5  Modification of extracted substance Animal

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying,micronisation

3.6 Quality Control Testing

3.6.2  Microbiological testing excluding sterility testing

3.6.1  Physical / Chemical testing

Active Substance:TRIAMCINOLONE HEXACETONIDE STERILE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
crystallisation

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.6 Quality Control Testing

3.6.4  Biological Testing

3.6.3  Microbiological testing including sterility testing

3.6.1  Physical / Chemical testing

Active Substance:FLUDROXYCORTIDE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:FLUOCINOLONE ACETONIDE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying,micronisation

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:FLUTICASONE PROPIONATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

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

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:TRIAMCINOLONE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:TRIAMCINOLONE ACETONIDE STERILE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.4 Manufacture of sterile Active Substance

3.4.1  Aseptically prepared

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying, micronisation

3.6 Quality Control Testing

3.6.4  Biological Testing

3.6.3  Microbiological testing including sterility testing

3.6.1  Physical / Chemical testing

Active Substance:METHYLPREDNISOLONE ACETATE STERILE

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:
crystallisation

3.4 Manufacture of sterile Active Substance

3.4.1  Aseptically prepared

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying, micronisation

3.6 Quality Control Testing

3.6.4  Biological Testing

3.6.3  Microbiological testing including sterility testing

3.6.1  Physical / Chemical testing

Active Substance:ISOPROTERENOL HYDROCHLORIDE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
crystallisation

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.6 Quality Control Testing

3.6.2  Microbiological testing excluding sterility testing

3.6.1  Physical / Chemical testing

Active Substance:NORURSODEOXYCHOLIC ACID

3.2 Extraction of Active Substance from Natural Sources

3.2.6  Purification of extracted substance Animal

3.2.5  Modification of extracted substance Animal

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.6 Quality Control Testing

3.6.2  Microbiological testing excluding sterility testing

3.6.1  Physical / Chemical testing

Active Substance:PARAMETHASONE ACETATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
crystallisation

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the 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

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:BUSULFAN

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Cytotoxic

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.4  Biological Testing

3.6.2  Microbiological testing excluding sterility testing

3.6.1  Physical / Chemical testing

Active Substance:SALMETEROL XINAFOATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
crystallisation

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.6 Quality Control Testing

3.6.2  Microbiological testing excluding sterility testing

3.6.1  Physical / Chemical testing

Active Substance:CLOBETASOL PROPIONATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying,micronisation

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:BECLOMETASONE DIPROPIONATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
purification

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:DESONIDE DISODIUM PHOSPHATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:MIVACURIUM CHLORIDE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.4  Biological Testing

3.6.2  Microbiological testing excluding sterility testing

3.6.1  Physical / Chemical testing

Active Substance:LOTEPREDNOL ETABONATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:METHYLPREDNISOLONE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
crystallisation

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying,micronisation

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:TRIAMCINOLONE ACETONIDE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying,micronisation

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:CYPROTERONE ACETATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:DIFLORASONE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:MEDROXYPROGESTERONE ACETATE STERILE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying

3.6 Quality Control Testing

3.6.4  Biological Testing

3.6.3  Microbiological testing including sterility testing

3.6.1  Physical / Chemical testing

Active Substance:BECLOMETASONE DIPROPIONATE STERILE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.4 Manufacture of sterile Active Substance

3.4.1  Aseptically prepared

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying, micronisation

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:BUDESONIDE STERILE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.4 Manufacture of sterile Active Substance

3.4.1  Aseptically prepared

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying, micronisation

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:CANNABIDIOL (SYNTHETIC)

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
crystallisation

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:LOTEPREDNOL ETABONATE STERILE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates
Special Requirements:
7.Other:
Other: Hormones or substances with hormonal activity

3.1.3  Salt formation / Purification steps:
crystallisation

3.4 Manufacture of sterile Active Substance

3.4.1  Aseptically prepared

3.5 General Finishing Steps

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.5.1  Physical processing steps:
drying, micronisation

3.6 Quality Control Testing

3.6.3  Microbiological testing including sterility testing

3.6.1  Physical / Chemical testing

Active Substance:CYSTEAMINE BITARTRATE MONOHYDRATE

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
crystallisation

3.1.2  Manufacture of crude active substance

3.1.1  Manufacture of active substance intermediates

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying

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)

3.5.2  Primary Packaging (enclosing / sealing the active substance within a packaging material which is in direct contact with the substance)

3.6 Quality Control Testing

3.6.2  Microbiological testing excluding sterility testing

3.6.1  Physical / Chemical testing

4. Other Activities - Active Substances:
Importation of: CHOLIC ACID (confidential), BETAMETHASONE (confidential), HYDROCORTISONE (confidential), METHYLPREDNISOLONE, PREDNISOLONE (confidential), TESTOSTERONE (confidential)

Clarifying remarks (for public users):

Manufactured active substances (AS) marked as confidential are for clinical use. Imported active substances (AS) marked as confidential undergo further processing within the importing site. Terminal sterilization by gamma irradiation is outsourced for MEDROXYPROGESTERONE ACETATE STERILE and TRIAMCINOLONE HEXACETONIDE STERILE and as an alternative even for BECLOMETASONE DIPROPIONATE STERILE. According to Italian legislation, all the sterile active substances and/or biological active substances and/or active substances deriving from human and animal tissues, organs, fluids are authorized according to art. 40 of Dir. 2001/83/EC and the production process is performed in accordance with the EU-GMP, including its Annex 1, as laid down in Dir. 2003/94/EC. On a risk-based approach, the validity of the GMP certificate for this manufacturing site is not more than 30 months from the latest general GMP inspection conducted on 2021/10/01, except for AIFA's re-evaluation of the risk profile.

The EudraGMDP database is maintained and operated by the EMA. Access to the general public is granted in order to enhance availability of information related to the EMA mandate. The content of the database is provided by the National Competent Authorities (NCA) of the EEA. For this reason, the EMA accepts no responsibility or liability whatsoever (including but not limited to any direct or consequential loss or damage it might occur to you and/or any other third party) arising out of or in connection with the information on this database. Any questions about the content should be addressed to the relevant NCA. Please click here to get list of NCA's.

For the UK, as from 1.1.2021, EU Law applies only to the territory of Northern Ireland (NI) to the extent foreseen in the Protocol on Ireland/NI.

Documents issued by UK authorities up to and including 31 December 2020 remain available for consultation in EudraGMDP. However, they are no longer included or updated from 1 January 2021, with the exception of the documents pertaining to sites located in Northern Ireland.