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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: 06-24-2026Quality 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: 05-18-2026Increase in STI consultations in 2023, rise in gonorrhoea cases persists
https://www.rivm.nl/en/news/increase-in-sti-consultations-in-2023-rise-in-gonorrhoea-cases-persists… were 89,386 STI consultations in the first half of 2023, marking a 12% increase from the first half of 2022. … Among heterosexual men, there were 478 cases of gonorrhoea, marking a 20% increase. The detection rate – the percentage …
Publication date: 11-23-2023Illegal 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