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Austrian Federal Office For Safety In Health Care

CERTIFICATE NUMBER: 482018-103855551

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
Art. 94(1) of Regulation (EU) 2019/6 as amended

The competent authority of Austria confirms the following:

The manufacturer: Velalabs GmbH

Site address:

Brunner Strasse 69/3, Liesing, Vienna, 1230

OMS Organisation Id. / OMS Location Id.: ORG-100032228 / LOC-100050404

Other

(Human) API-A123(6)-R2019/6/EU,API-A111(1)-D2001/83/EC,NIP-A40-D2001/83/EC

(Veterinary) NIP-A88-R2019/6/EU

(Investigational product) NIP-A61-R2014/536/EU

From the knowledge gained during inspection of this manufacturer, the latest of which was conducted on 2024-03-21 , 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 and guidelines of Good Manufacturing Practice laid down in Directive 91/412/EEC. (3)

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, Art. 111(5) of Directive 2001/83/EC and Art. 80(5) of Directive 2001/82/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
Veterinary Medicinal Products

1 MANUFACTURING OPERATIONS

1.1 Sterile products

1.1.3 Batch certification

1.3 Biological medicinal products (list of product types)

   1.3.2  Batch Certification (list of product types)
           1.3.2.2  Immunological products
           1.3.2.5  Biotechnology products

1.4 Other products or manufacturing activity

1.4.3 Other: Lagerung von Master Cell Banks (MCB) und Working Cell Banks (WCB) im Kundenauftrag / Storage of Master Cell Banks (MCB) and Working Cell Banks (WCB) for customer(s) , Lagerung von Master Cell Banks (MCB) und Working Cell Banks (WCB) im Kundenauftrag / Storage of Master Cell Banks (MCB) and Working Cell Banks (WCB) for customer(s)(en)

1.6 Quality control testing

   1.6.1  Microbiological: sterility
   1.6.2  Microbiological: non-sterility
   1.6.3  Chemical/Physical
   1.6.4  Biological

2 IMPORTATION OF MEDICINAL PRODUCTS

2.1 Quality control testing of imported medicinal products

   2.1.1  Microbiological: sterility
   2.1.2  Microbiological: non-sterility
   2.1.3  Chemical/Physical
   2.1.4  Biological

2.2 Batch certification of imported medicinal products

   2.2.1  Sterile products
           2.2.1.1  Aseptically prepared
           2.2.1.2  Terminally sterilised
   2.2.3  Biological medicinal products
           2.2.3.2  Immunological products
           2.2.3.5  Biotechnology products

2.3 Other importation activities

2.3.4 Other: Lagerung von Master Cell Banks (MCB) und Working Cell Banks (WCB) im Kundenauftrag / Storage of Master Cell Banks (MCB) and Working Cell Banks (WCB) for customer(s), Lagerung von Master Cell Banks (MCB) und Working Cell Banks (WCB) im Kundenauftrag / Storage of Master Cell Banks (MCB) and Working Cell Banks (WCB) for customer(s)(en)

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

[900000005572]The complete list of APIs that are subject to quality control testing is available to the Austrian Federal Office for Safety in Health Care (BASG/AGES)(en)

3. MANUFACTURING OPERATIONS - ACTIVE SUBSTANCES

Active Substance:The complete list of APIs that are subject to quality control testing is available to the Austrian Federal Office for Safety in Health Care (BASG/AGES)

3.6 Quality Control Testing

3.6.1  Physical / Chemical testing

3.6.3  Microbiological testing including sterility testing

3.6.4  Biological Testing

Clarifying remarks (for public users):

Velalabs GmbH; ad 1.1, 1.3 und 2.2 eingeschränkt auf Omalizumab Injection (ADL-018) / ad 1.1, 1.3 and 2.2 restricted to Omalizumab Injection (ADL-018) Betreffend folgende Verfahren Probebetrieb bis 31.03.2027 / Regarding the following inspection cases valid until 31.03.2027:INS-482018-103279141 INS-482018-103855551

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.