Meet our leading experts and experience BSI's commitment to maintaining quality and delivering excellence.
Our leading experts will share their knowledge and collaborate to advance healthcare regulatory practice at RAPS Euro Convergence 2026. With in-depth sessions and interactive workshops, our team will be providing valuable insights to navigate the evolving regulatory landscape.
BSI Medical Devices offers a comprehensive regulatory services portfolio to place your product on the market
As a leading full scope Notified Body and UK Approved Body, our comprehensive services encompass every aspect of regulatory compliance. Our service include:
- CE certification
- UKCA certification
- Structured Dialogue
- ISO 13485 Quality Management System (QMS)
- MDSAP Certification – Medical Device Single Audit Program
- ISO 42001 AI Management System
- Medical Device Regulation (MDR)
- In Vitro Diagnostic Regulation (IVDR)
- Interactive Dedicated reviews
Meet us at booth B39-40 to discover how our comprehensive regulatory services portfolio, combined with our world-leading experience, provides you with efficient pathways to bring your device to market.
