• Inicio
  • Formações
  • Formação à Medida
  • News & Trends
  • Sobre nós
  • Contacto

Updated: ICH Q12: A Framework for Managing Post-Approval CMC Changes

The US Food and Drug Administration (FDA) made available an International Council for Harmonisation (ICH) draft guidance on technical and regulatory considerations for pharmaceutical lifecycle management.

Q12 Technical and Regulatory Considerations for Pharmaceutical Product Lifecycle Management

Q12 Annex

News & Trends

Procurar

Recentes

  • 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
  • BOAS PRÁTICAS de FARMACOVIGILÂNCIA : ” Formação completa, contempla os pontos principais de Boas Práticas de Farmacovigilância “

91 257 00 03 (Chamada para a rede móvel nacional)
info@formiventos.com

  • Follow
  • CLIENTES & TESTIMONIALS
  • ASSOCIAÇÕES OFICIAIS
  • CERTIFICAÇÕES E CREDITAÇÕES
  • ADVISORY BOARD
  • Política de Privacidade
  • Contacto