Recentes

• Update to EU GMP Guidelines – Revised Annex 19 on Reference and Retention Samples
• FARMACOVIGILÂNCIA nível avançado : Formação completa con casos práticos
• FDA DRAFT GUIDANCE :Demonstrating Substantial Evidence of Effectiveness for Human Drug and Biological Products
• European Biotech Act: Positioning EU as Biotech Powerhouse
• CIOMS Glossary of ICH Terms and Definitions. Version 10
• Guidance on standardisation for medical devices Appendix: Transition to the ‘EU REP’ symbol in EN ISO 15223-1
• MDCG Position Paper: Management of SS(C)P in EUDAMED after mandatory use
• Commission Implementing Decision amending Implementing Decision (EU) 2021/1195 as regards the harmonised standard for symbols to be used with information to be supplied by the manufacturer