EudraVigilance training and support

The European Medicines Agency (EMA) offers training to support stakeholders in meeting their pharmacovigilance obligations when using EudraVigilance. Training is important to ensure that users understand its functionalities and submit high quality data which adhere to standards that allow for adequate monitoring of the safety of medicines and the...

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HumanRegulatory and procedural guidancePharmacovigilanceResearch and development
Biologicals: finished product

The European Medicines Agency's scientific guidelines on biological medicinal products help medicine developers prepare marketing authorisation applications for human medicines.

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HumanBiologicalsRegulatory and procedural guidanceResearch and developmentScientific guidelines
Quality: specific types of products

The European Medicines Agency's scientific guidelines on specific types of products help medicine developers prepare marketing authorisation applications for human medicines.

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HumanRegulatory and procedural guidanceQuality of medicinesResearch and developmentScientific guidelines
Academia Info Day
European Medicines Agency, Amsterdam, the Netherlands
Start date: 10 November 2023, 09:30 (CET)
End date: 10 November 2023, 13:30 (CET)
EventHumanCorporateResearch and development
Research and development (veterinary medicines)

The European Medicines Agency (EMA) provides guidance and support to companies researching and developing veterinary medicines. This includes scientific and regulatory information on how to design and run clinical trials, compliance standards, how to establish maximum residue limits for medicines and biocides, support to innovation, and support the...

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Research and development