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Landesamt Fuer Gesundheit Und Soziales

CERTIFICATE NUMBER: DE_BE_01_GMP_2026_0059

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

Part 1

Issued following an inspection in accordance with
Art. 63 of Regulation (EU) 536/2014 as amended
Art. 111(5) of Directive 2001/83/EC as amended

The competent authority of Germany confirms the following:

The manufacturer: Chemisch-pharmazeutisches Labor Rolf Sachse GmbH

Site address:

Stieffring 14, Charlottenburg, Berlin, 13627, Germany

OMS Organisation Id. / OMS Location Id.: ORG-100013251 / LOC-100022210

Has been inspected under the national inspection programme in connection with manufacturing authorisation no. DE_BE_01_MIA_2026_0019 in accordance with Art. 61 of Regulation (EU) No 536/2014 and Art. 40 of Directive 2001/83/EC, transposed in the following national legislation:Sect. 13 para 1 German Medicinal Product Act (manufacture) and § 72 German Medicinal Product Act (import).

Is an active substance manufacturer that has been inspected in accordance with Art. 111(1) of Directive 2001/83/EC1 transposed in the following national legislation:Sect. 64 para 1 and 3 German Medicinal Product Act.

Other

(Human) analytische Prüfung von Humanarzneimitteln sowie klinischen Prüfpräparaten und Wirkstoffhersteller

From the knowledge gained during inspection of this manufacturer, the latest of which was conducted on 2026-03-25 , it is considered that it complies with:

The principles and guidelines of Good Manufacturing Practice laid down in Directive (EU) 2017/1572 and/or Commission Delegated Regulation (EU) 2017/1569, as reflected by the product categories stated in Part 2. (3)

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 transposed in the following national legislation:Sect. 64 para 1 and 3 German Medicinal Product Act.

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. 15 of Directive 2001/20/EC and 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
Human Investigational Medicinal Products

1 MANUFACTURING OPERATIONS

1.6 Quality control testing

1.6.3 Chemical/Physical

2 IMPORTATION OF MEDICINAL PRODUCTS

2.1 Quality control testing of imported medicinal products

2.1.3 Chemical/Physical

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

[00026665-00001]Anagrelide hydrochloride(en)

[00026665-00002]Clenbuterol hydrochloride(en)

[00026665-00003]Methacetin (C 13)(en)

[00026665-00004]Nabilone(en)

[00026665-00005]Phenoxybenzamine hydrochloride(en)

[00026665-00006]Atipamezol hydrochloride(en)

3. MANUFACTURING OPERATIONS - ACTIVE SUBSTANCES

Active Substance:Anagrelide hydrochloride

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
cristalisation and filtration

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying and homogenization

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:Clenbuterol hydrochloride

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
cristalisation and filtration

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying and homogenization

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:Methacetin (C 13)

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
cristalisation and filtration

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying and homogenization

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:Nabilone

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
cristalisation and filtration

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying and homogenization

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:Phenoxybenzamine hydrochloride

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
cristalisation and filtration

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying and homogenization

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Active Substance:Atipamezol hydrochloride

3.1 Manufacture of Active Substance by Chemical Synthesis

3.1.3  Salt formation / Purification steps:
cristalisation and filtration

3.5 General Finishing Steps

3.5.1  Physical processing steps:
drying and homogenization

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

Clarifying remarks (for public users):

The authorisation is based on floor plans No.1 and No.2 from July 10th 2026 and is dedicated to analytical testing procedures of medicinal products only. to 1.6.3 und 2.1.3: The authorised testing activities do not include batch certification.

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.