Una Sherye

Medical Device Regulatory Conferences 2024. Overcome your eu mdr, ivdr, regulatory affairs in global markets, clinical, pms, medical law & compliance, biocompatibility, and software & ai for medical devices with expert guidance from eu commission, competent authorities, notified bodies and. We will cover challenges in regulatory pathways that need to be addressed to ensure the final commercial success of a product.

Thank you to those who participated in the inaugural aami/fda. Prepare for the 2027/ 2028 transition deadline with key learnings from the eu commission, notified bodies and medical device manufacturers on the eu mdr, ukca, and meddo.