News & Trends
Procurar
Recentes
- webinar INTELIGÊNCIA ARTIFICIAL NA INDÚSTRIA FARMACÊUTICA :IA EM CONTEXTO GxP (Annex 11, 22, EU AI Act , GAMP®)
- GESTÃO da DISPONIBILIDADE do MEDICAMENTO: “Formação muito útil !
- IMDRF Playbook for Medical Device Regulatory Reliance Programs
- IMDRF Considerations for the selection of IMDRF Adverse Event Terminology
- Concept paper on the revision of the guidelines on Good Manufacturing Practice for medicinal products – Annex 15 – Qualification and Validation
- FDA Draft Guidance General Considerations for Patient Preference Studies February 2026
- Open consultation: Medical devices regulations: targeted consultation on the indefinite recognition of CE marked devices
- Health Technology Assessment: HTA 2025 Annual Report