Description
NAMSA invites you to join us at MedTech Summit (Informa) on June 16-20, 2025 in Berlin, Germany!
About the Meeting:
” Where the MedTech Regulatory Industry Meets The Leading Medical Device and IVD Regulatory Affairs Event in Europe. Master the End-To-End Certification Pathway. Streamline Global Market Access. Maintain Compliance. With Expert Guidance from Competent Authorities, Notified Bodies and Industry.”
Presentation
Topic: “The Paper Anniversary: 1 Year on since ISO 10993-17.”
With –17 having been in place for 1 year, what are industry’s first experiences of adhering to the standard?
- Are there differences in EU and FDA acceptance?
- Can we expect further alignment?
- Which parts are causing the most confusion?
- Possible solutions to ease working under -17
Time: June 18, 2025 at 11:10
Speaker: Kim Ehman; Director of Regulatory Toxicology; NAMSA
COMPLIMENTARY CONSULTATIONS
Visit our booth 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 email us at communications@namsa.com to reserve your consultation time, or simply stop by the booth in the exhibitor area to meet with us. We hope to see you there!
Register on Event Website
