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You searched for these word(s): markControl of medicines
https://www.rivm.nl/en/medicinal-products/control-of-medicines… Once it is authorised on the market, a chemical medicinal product may be subject to … the active ingredient content as registered in the marketing authorization application or in the legal … The Centrally Authorised Products programme of the EMA The Market Surveillance Study programme of the EDQM (not …
Publication date: 06-24-2026The 'SPARK' project studying pesticides and Parkinson’s
https://www.rivm.nl/en/bestrijdingsmiddelen/spark… progressively die off over time. Before placement on the market in the European Union (EU), EU Regulation No.283/2013 … neurodegenerative diseases: possibilities for improving the market authorisation requirements (in Dutch) … about the approval of these chemical substances for the market. Collaboration The RIVM seeks advice from external …
Publication date: 06-11-2025Quality and control
https://www.rivm.nl/en/medicinal-products/quality-control… Monitoring the quality of medicines on the market is a continuous process. Prior to the market authorization, the quality assessment is based on the … all registered medicines is in order. Before and/or after market authorization, research takes place. The aim is to …
Publication date: 05-18-2026Illegal medicines
https://www.rivm.nl/en/medicinal-products/illegal-medicines… (manufacturer, country of production, country of origin or marketing authorization holder) or history (registries or … Board) and the EMA (European Medicines Agency) issue the marketing authorisations for medicines. Falsified medicines …
Publication date: 05-18-2026Release of plasma-derived medicines and vaccines
https://www.rivm.nl/en/medicinal-products/release-of-plasma-derived-medicines-and-vaccines… bacteria or toxins. If a faulty product enters the market, consequences can be great, both for the individual … of the OCABR procedure Batch release request forms: Marketing Information Form Request for OCABR Other …
Publication date: 06-24-2026