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PLANOS DE CONTINGÊNCIA /BUSINESS CONTINUITY em Farmacovigilância
Lisboa , 21 de abril de 2026
GVP advanced : FARMACOVIGILÂNCIA nível avançado
Lisboa , 23 de junho de 2026
AUDITORIAS DE FARMACOVIGILÂNCIA a SERVICE PROVIDERS
Lisboa, 26 de novembro
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Recentes
EMA’s ePI Roadmap
Sponsor Frequently Asked Questions Clinical Trial Information System (CTIS) Frequently Asked Questions (FAQs) on the Sponsor’s workspace
The new CTIS Sponsor Handbook (v6.2, March 2026)
New revision of the Q&A document on art. 10(a) interruption of supply published
IMDRF Technical Framework for Artificial Intelligence Life Cycle Management” (IMDRF AIML WG N93 – April 2026)
New Harmonised Standards under MDR – April 2026
EMA/CHMP: Updated Guideline on Active Substances published
Data Quality Framework for EU medicines regulation: application to Real-World Data