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Recentes
- 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
- BOAS PRÁTICAS de FARMACOVIGILÂNCIA : ” Formação completa, contempla os pontos principais de Boas Práticas de Farmacovigilância “
- New EMA GMP Guidelines in the next three Years : The 3-year work plan for the Inspectors Working Group
- Formação QUALITY MANAGEMENT SYSTEM: ” Ótima forma de rever temas e aprofundar conhecimentos com casos do dia -a-dia “
- C(2026) 1809 expands the list of Class IIb implantable devices exempt from the obligation to perform an assessment of technical documentation for every device under Article 52(4).
- EU PARLIAMENT Textes Adopted on AI – 26/03/2026 Simplification of the implementation of harmonised rules on artificial intelligence (Digital Omnibus on AI)