Artigos recentes
- European Medicines Agency post-authorisation procedural advice for users of the centralised procedure
- Quality documentation for medicinal products when used with a medical device- effective from 1/01/2022
- Artificial intelligence in medicine regulation
- Clinical Trial Information System (CTIS) – Sponsor Handbook
- Sistema europeu de ensaios clínicos lançado em janeiro
- EMA new guidelines on veterinary pharmacovigilance
- Veterinary product information templates
- MDCG 2021-19 Guidance note integration of the UDI within an organisation’s quality management system