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Austrian Federal Office For Safety In Health Care

CERTIFICATE NUMBER: 480934-103646945

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

Part 1

Issued following an inspection in accordance with
Art. 94(1) of Regulation (EU) 2019/6 as amended
Art. 111(5) of Directive 2001/83/EC as amended

The competent authority of Austria confirms the following:

The manufacturer: Elisabeth Schubert Soft-Line Chemisch-Technische Produkte Nea Warenvertriebsgesellschaft mbH

Site address:

Schumanngasse 74, Hernals, Vienna, 1170, Austria

OMS Organisation Id. / OMS Location Id.: ORG-100024672 / LOC-100033856

Has been inspected under the national inspection programme in connection with manufacturing authorisation no. 480934 in accordance with Art. 40 of Directive 2001/83/EC, transposed in the following national legislation:§ 63 Medicines Act (Arzneimittelgesetz) and Ordinance 2009 (Arzneimittelbetriebsordnung 2009).

Is an active substance manufacturer that has been inspected in accordance with Art. 123(6) of Regulation (EU) 2019/6 and Art. 111(1) of Directive 2001/83/EC1 transposed in the following national legislation:§ 63a Medicines Act (Arzneimittelgesetz) and Ordinance 2009 (Arzneimittelbetriebsordnung 2009).

From the knowledge gained during inspection of this manufacturer, the latest of which was conducted on 2025-05-13 , it is considered that it complies with:

The principles and guidelines of Good Manufacturing Practice laid down in Directive (EU) 2017/1572. (3)

The principles and guidelines of Good Manufacturing Practice laid down in Directive 91/412/EEC. (3)

The principles of GMP for active substances referred to in Art. 123(6) of Regulation (EU) 2019/6 and 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:§ 63a Medicines Act (Arzneimittelgesetz) and Ordinance 2009 (Arzneimittelbetriebsordnung 2009).

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. 80(5) of Directive 2001/82/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
Veterinary Medicinal Products

1 MANUFACTURING OPERATIONS

1.5 Packaging

   1.5.1  Primary Packaging
           1.5.1.17  Other non-sterile medicinal products: Other non-sterile medicinal products Zubereitungen gemäß den Arzneibüchern/ Preparations according to pharmacopoeia(en)
   1.5.2  Secondary packaging

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

[900000005552]Die vollständige Liste der hergestellten und/oder in Verkehr gebrachten und/oder importierten Wirkstoffe ist dem Bundesamt für Sicherheit im Gesundheitswesen (BASG/AGES) bekannt / The complete list of manufactured and/or distributed and/or imported active substances is available at the Austrian Federal Office for Safety in Healthcare (BASG/AGES)(en)

3. MANUFACTURING OPERATIONS - ACTIVE SUBSTANCES

Active Substance:Die vollständige Liste der hergestellten und/oder in Verkehr gebrachten und/oder importierten Wirkstoffe ist dem Bundesamt für Sicherheit im Gesundheitswesen (BASG/AGES) bekannt / The complete list of manufactured and/or distributed and/or imported active substances is available at the Austrian Federal Office for Safety in Healthcare (BASG/AGES)

3.5 General Finishing Steps

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

3.5.3 Secondary Packaging (placing the sealed primary package within an outer packaging material or container. This also includes any labelling of the material which could be used for identification or traceability (lot numbering) of the active substance)

Clarifying remarks (for public users):

Hersteller Wirkstoffe: Elisabeth Schubert Soft-Line Chemisch-Technische Produkte Nea Warenvertriebsgesellschaft mbH; Die vollständige Liste der hergestellten und/oder in Verkehr gebrachten Wirkstoffe ist dem Bundesamt für Sicherheit im Gesundheitswesen (BASG/AGES) bekannt. / The complete list of manufactured and/or distributed active substances is available at the Austrian Federal Office for Safety in Healthcare (BASG/AGES). Befristet bi…; Hersteller Arzneimittel: Elisabeth Schubert Soft-Line Chemisch-Technische Produkte Nea Warenvertriebsgesellschaft mbH; Befristet bis zum /valid until: 30.06.2027;

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.