The MDR and IVDR changes have added new requirements around clinical evaluation, risk management, and post-market surveillance, which continue to impact the regulatory affairs profession in Europe and elsewhere. Attending this conference will provide regulatory affairs professionals in medical devices with actionable solutions for these three pillars.
Programme |
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Nearly 20 education sessions with today's leading regulatory experts. |
Registration is now open! Don't miss out on this exciting program. Early pricing ends 27 September 2024. |
RAPS has negotiated discounted hotel rates for the conference. Reserve early, the booking deadline is 2 September. |