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You searched for these word(s): markQuality 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: 05-18-2026Next milestone in universal PFAS restriction process completed
https://www.rivm.nl/en/news/next-milestone-in-universal-pfas-restriction-process-completed… from five countries (Germany, the Netherlands, Norway, Denmark and Sweden) have taken into account the feedback of … authorities from Germany, the Netherlands, Norway, Denmark and Sweden, in the following referred to as Dossier … as whether derogations are required for the second-hand market, recycling and spare parts. Additionally, eight …
Publication date: 08-26-2025