Medical Device Regulatory Conferences 2024. Click on the session title for more details. Overcome your eu mdr, ivdr, regulatory affairs in global markets, clinical, pms, medical law & compliance, biocompatibility, and software & ai for.
Optimize your regulatory oversight with perspectives from notified bodies and industry peers. Clarification of regulatory requirements for companion diagnostics & ngs, insight into the status of laboratory developed test specific policies, all while strategizing to ensure.