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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: 05-18-2026Application in products
https://www.rivm.nl/en/nanotechnology/application-in-products… level. Such substances may only be introduced to the market if they have received approval. … nanomaterial is safe; otherwise, the manufacturer may not market it. Research shows that companies do not always …
Publication date: 07-19-2012Laws and regulations
https://www.rivm.nl/en/nanotechnology/laws-and-regulations… that manufacturers and importers introduce to the European market must be safe, including advanced materials. The …
Publication date: 07-19-2012