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Last updated 7 days ago
7 days ago
PRIME eligibility requests: 2025 deadlines for submission and timetable for assessment
20 days ago
List of centrally authorised products with safety-related changes to the Product Information
21 days ago
EU Individual Case Safety Report (ICSR) implementation guide business rules spreadsheets
22 days ago
Management of rapid alerts arising from quality defects risk assessment
22 days ago
History of changes to the compilation of procedures
about 1 month ago
Superseded - EMA guidance on the use of medicinal products for the...
about 1 month ago
EMA guidance on the use of medicinal products for treatment in case...
about 1 month ago
Superseded - EMA guidance on use of medicinal products for the treatment...
about 1 month ago
EMA guidance on the use of medicinal products for treatment and prophylaxis...
about 1 month ago
Scientific advice under Article 115(5) of Regulation (EU) 2019/6 on veterinary medicinal...
about 1 month ago
Scientific advice under Article 115(5) of Regulation (EU) 2019/6 on veterinary medicinal...
about 2 months ago
Guideline on good pharmacovigilance practices (GVP) Module XVI – Risk minimisation measures...