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European Biotech Act: Potential new extension for supplementary protection certificates (SPCs) for ATMPs and biotechnology medicines
European Commission Announces (Long Awaited) Proposal to Simplify EU Medical Device Regulations
MHRA Announces Consultation Response on Reforms to GB Pre-Market Medical Device Regulation
The Covington European Life Sciences Symposium 2025
EMA Clinical Data Publication Policy to Cover All New Marketing Authorization Applications, Line Extensions and Major Clinical Type II Variations Starting Q2 2025
EU Talking Life Sciences Audiocast: WHO Prequalification Procedures in Africa
UK HRA Consults on a New Model Investigator-Initiated Study Agreement