Recentes

• Study supporting the monitoring of the availability of medical devices on the EU market
• GDP AUDITS 2026 : “Tema muito bem explicado , com a resolução de casos práticos”
• MDR/IVDR Revision: A Regulatory System at a Crossroads
• EMVO Systems Updates | May 2026
• EU agrees to simplify AI rules to boost innovation and ban ‘nudification’ apps to protect citizens
• Formação DIGITAL PROMO REVIEW : ” Formação muito interativa , bem estruturada e com elevada partilha de casos práticos “
• Best Practice Guidance for the Submission of Technical Documentation under Annex II and III of Medical Device Regulation
• COMMISSION IMPLEMENTING REGULATION laying down certain uniform quality management and procedural requirements for the conformity assessment activities carried out by a notified body designated