Swissmedic licence

Max Zeller Söhne AG

Swissmedic licence 512100-102709003 · Romanshorn · COMPLIANT

Key facts

Authorization number 512100-102709003
Licence holder Max Zeller Söhne AG
Site Max Zeller Söhne AG
City Romanshorn
Canton TG
Country Switzerland
Compliance status COMPLIANT
Last inspection Feb 16, 2024
Valid until Indefinite
Manufacturing activities 1 MANUFACTURE OF MEDICINAL PRODUCTS (WITHOUT LABILE BLOOD PRODUCTS), 1.2 Non-sterile products, 1.2.1 Non-sterile products (processing operations for the following dosage forms), 1.2.1.6 Liquids for internal use (H/V,I), 1.2.1.8 Other solid dosage forms (H/V,I), 1.2.1.11 Semi-solids (H/V,I), 1.2.1.13 Tablets (H/V,I), 1.2.2 Batch certification (technical release) (H/V,I), 1.4 Other products or manufacturing activity, 1.4.1 Manufacture of:, 1.4.1.1 Herbal products (H/V,I), 1.5 Packaging and 7 more
Wholesale activities S.4 WHOLESALE DISTRIBUTION OF MEDICINAL PRODUCTS (WITHOUT LABILE BLOOD PRODUCTS), S.4.1 Wholesale distribution of non- ready-to-use medicinal products, S.4.1.1 Medicinal products (intermediates, without immunological and blood products) (H/V,I), S.4.1.4 Active substances (H/V,I), S.4.2 Wholesale distribution of ready-to-use medicinal products, including market release, S.4.2.1 Medicinal products (without immunological and blood products) (H/V,I), S.4.6 Outsourcing of manufacture of medicinal products as contract giver (H/V)
Import activities S.2 IMPORT OF MEDICINAL PRODUCTS (WITHOUT LABILE BLOOD PRODUCTS), S.2.1 Import of non- ready-to-use medicinal products, S.2.1.1 Medicinal products (intermediates, without immunological and blood products) (H/V,I), S.2.1.4 Active substances (H/V,I), S.2.2 Import of ready-to-use medicinal products, including market release, S.2.2.1 Medicinal products (without immunological and blood products) (H/V), S.2.2.2 Immunological medicinal products (H/V), S.2.3 Import of ready-to-use medicinal products, excluding market release, S.2.3.1 Medicinal products (without immunological and blood products) (H/V,I), S.2.3.4 The import of ready-to-use medicinal products, excluding market release, is restricted to:, S.2.3.4.2 the import on behalf of the marketing authorisation holder (H/V), S.2.3.4.4 the import of medicinal products for clinical trials on behalf of the sponsor for subsequent distribution to the trial centres (I) and 1 more
Record type Medicinal Products
Swissmedic record swissgmdp.ch

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About Swissmedic establishment licences

Swissmedic licenses establishments that manufacture, import, export or distribute medicinal products in Switzerland and records their GMP/GDP compliance status.

Source: Swissmedic, Swiss Agency for Therapeutic Products

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