Gain Actionable Solutions in Clinical, Risk Management, and Postmarket Surveillance
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.
The European Clinical, Risk, and Postmarket Surveillance Conference is developed and curated by the RAPS European Council (REC).
Dates
22 October 2024 - Preconference Workshop
23-24 October 2024- Main Conference
Registration Fees & Deadlines
Preconference Workshop Pricing
Until 27 September 2024: Member 610 EUR | Nonmember 720 EUR
28 September 2024 - 22 October 2024: Member 670 EUR | Nonmember 795 EUR
Main Conference Pricing
Until 27 September 2024: Member 1,045 EUR | Nonmember 1,235 EUR
28 September 2024 - 23 October 2024: Member 1,235 EUR | Nonmember 1,445 EUR
Accommodations & Travel Information
AC Hotel Barcelona Forum
Pg. del Taulat, 278
Sant Martí
08019 Barcelona, Spain
Reserve your room
Cancellations and Refunds
All requests for cancellations must be received in writing at support@raps.org by 11:59 pm ET on 23 September 2024 and are subject to an assessment fee according to the schedule below:
- Requests received by 23 June at 11:59 pm ET will be assessed a 10% fee.
- Requests received between 24 June and 27 August at 11:59 pm ET will be assessed a 20% fee.
- Requests received between 28 August and 23 September will be assessed a 50% fee. Cancellations received after 23 September will be non-refundable, except in cases of documented medical emergencies.
Refunds will not be issued for no-shows.