RAPS Euro Convergence 2024

NAMSA invites you to join us for the RAPS Euro Regulatory Convergence Conference on 6-8 May in Berlin. Come together with other European regulatory affairs professionals to discuss pressing regulatory topics and share best practices within the MedTech industry.

NAMSA EDUCATIONAL SESSION

Effective Strategies When Approaching Regulatory Due Diligence under the MDR
presented by Matt Royle, PhD; Principal Regulatory Consultant
8 May | 13:15 – 13:45 CEST

What can Manufacturers Learn from Effective PMS/PMPF Strategies to Strengthen their Clinical Evidence with the IVDR Transition Deadline Approaching?
presented by Warren Jameson, PhD; Senior Manager, Regulatory & Quality
7 May | 12:30 – 13:00 CEST

Innovation vs Legacy: Scientific Validity vs a New Scientific Concept to be Novel in an IVDR Environment
presented by Warren Jameson, PhD; Senior Manager, Regulatory & Quality
7 May | 16:45 – 17:45 CEST

UK Market: PMS and Vigilance Requirements for IVDs
presented by Christèle East, PhD; Senior Regulatory Consultant
7 May | 11:30 – 12:00 CEST

Substances of Concern – Have You Checked? GSPR 10.4: A Practical Guide
presented by to be confirmed
7 May | 8:30 – 9:30 CEST

Medical Devices Utilizing Animal Tissues – Impact of the MDR and the Pandemic
presented by Jane Arnold-Round, MSC; Senior Principal Consultant
Poster Presentation

COMPLIMENTARY CONSULTATIONS
Visit us at Booth B15 for complimentary 30-minute consultations with NAMSA’s experts throughout the event. We welcome the opportunity to discuss with you the most cost-effective pathways to market based on your unique product development requirements.

Please contact us to reserve your consultation time.