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necessary Change in the name of a human medicinal product due to a change of ownership according to Art 25 Medicinal Products Act (Arzneimittelgesetz AMG ) must be submitted as a separate variation according [...] Art 16 TAMG (veterinary) Change of Ownership/Transfer of Title for marketing authorisations and registrations according to Art 25 Medicinal Products Act (Arzneimittelgesetz AMG) (human) and Art 16 TAMG [...] classification A.2.b, type IB - in case of authorised products or according to Art 24 (2) Z1 Medicinal Products Act (Arzneimittelgesetz AMG ) for registered products. For veterinary medicinal products a VNRA –
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that places a device from a third country on the Union market. Distributor means any natural or legal person in the supply chain, other than the manufacturer or the importer, that makes a device available [...] distributor considers or has reason to believe that a device which it has placed on the market or made available on the market presents a serious risk or is a falsified device, it shall immediately inform the [...] including a description of the identified defects. For efficient communication regarding the follow-up of identified defects, you will receive a form with the inspection report, including a brief description
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