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- IMDRF/MC/N2FINAL:2025 (Edition 13) Standard Operating Procedures version 2
- New EU Regulation : Safer Cosmetics Ahead
- CIOMS proposes best practices for AI in pharmacovigilance
- AI Literacy – Questions & Answers
- ICH Guideline M13B on bioequivalence for immediate-release solid oral dosage forms – additional strengths biowaiver – Scientific guideline
- Concept paper on the revision of Part IV Guidelines on Good Manufacturing Practice specific to Advanced Therapy Medicinal Products
- GDP MED 2025 : Mais uma edição marcada pela excelencia em termos de qualidade e relevância dos conteúdos
- Team-NB Version 3 of Position Paper on the submission of technical documentation according to Annex II and III of the Medical Device Regulation