Recentes

• Product Management Services (PMS) – Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe
• AI Omnibus enters into force
• EU CTR Q&A Version 7.3 is Out
• New WHO guide on Artificial intelligence-related health research
• GDP for APIs: APIC Publishes Updated “How to Do” Document
• Team-NB Position Paper :TRANSFER AGREEMENT FOR SURVEILLANCE OF LEGACY DEVICES
• MDR Certification Process (including Pre-application, Application and Post Application phases) – Consensus document
• New ISO Guidance for AI-Powered Medical Devices: ISO/TS 24971-2:2026 Published!