Webinar: Complying with the EU Medical Device Regulation (MDR 2017/745)

The Medical Device Regulation (MDR 2017/745) is now fully enforced across the European Union, requiring rigorous conformity assessment, comprehensive technical documentation, and ongoing post-market surveillance. Manufacturers must maintain continuous compliance to uphold their CE marking and meet the high standards set by the regulation.

During this webinar, you will learn:

• How the MDR certification pathway works and what is required for compliance
• Key regulatory considerations for companies supplying EU and UK markets
• Typical timelines for conformity assessment and certificate issuance
• Intertek’s MDR (2017/745) accreditation scope as listed in NANDO
• How to plan effectively for audits, renewals, and ongoing regulatory obligations