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Austrian Agency For Health And Food Safety

CERTIFICATE NUMBER: 483041-105715126

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 Austria confirms the following:

The manufacturer: Takeda Manufacturing Austria AG

Site address:

Pasettistrasse 76, Brigittenau, Vienna, 1200

OMS Organisation Id. / OMS Location Id.: ORG-100000816 / LOC-100052070

Has been inspected under the national inspection programme in connection with manufacturing authorisation no. 483041 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:§ 63 Medicines Act (Arzneimittelgesetz) and Ordinance 2009 (Arzneimittelbetriebsordnung 2009).

From the knowledge gained during inspection of this manufacturer, the latest of which was conducted on 2024-02-28 , 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)

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

1.4 Other products or manufacturing activity

1.4.3 Other: Lagerung von Humanplasma zur Fraktionierung, Zwischenprodukten und Rohstoffen, Back-up zur Lagerung von Stabilitäts-, Rückstell- und Referenzproben / Storage of human plasma for fractionation, intermediate products and raw materials, back-up for stability-, reference- and retention-samples, Lagerung von Humanplasma zur Fraktionierung, Zwischenprodukten und Rohstoffen, Back-up zur Lagerung von Stabilitäts-, Rückstell- und Referenzproben / Storage of human plasma for fractionation, intermediate products and raw materials, back-up for stability-, reference- and retention-samples(en)

2 IMPORTATION OF MEDICINAL PRODUCTS

2.3 Other importation activities

   2.3.1  Site of physical importation
   2.3.2  Importation of intermediate which undergoes further processing
   2.3.4  Other: Humanplasma zur Fraktionierung / Human plasma for fractionation , Humanplasma zur Fraktionierung / Human plasma for fractionation(en)

Clarifying remarks (for public users):

Hersteller Arzneimittel: Takeda Manufacturing Austria AG; Mit 23.12.2021 wurde die Baxter AG in Takeda Manufacturing Austria AG umbenannt. / As of 23 December 2021 Baxter AG was renamed into Takeda Manufacturing Austria AG.; Hersteller klinischer Prüfpräparate: Takeda Manufacturing Austria AG; Mit 23.12.2021 wurde die Baxter AG in Takeda Manufacturing Austria AG umbenannt. / As of 23 December 2021 Baxter AG was renamed into Takeda Manufacturing Austria AG.;

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.