medical devices regulation

Regulatory Updates for Medical Device Certification

On-demand Webinar

On-demand Webinar

As the medical device industry continues to evolve, manufacturers need to stay up-to-date with the ever-changing landscape of regulatory requirements. With the recent regulatory updates, medical device manufacturers must comply with the updated requirements before bringing medical devices to market.

In this session, our expert will cover the recent regulatory updates and transitional period for MDR, IVDR and UKCA. This webinar will also discuss the compliance requirements and best practices to navigate the regulatory landscape.

Register now to learn about the importance of these regulatory requirements for the medical device industry and the timeline required for implementation. 

To view the webinar, fill up the form now. 


OUR WEBINAR WILL TACKLE THESE POINTS, FOCUSING ON:

  • Medical Device Regulation (MDR) & In-Vitro Diagnostic Regulation (IVDR)
    • Recent updates and actual possibilities
    • Transitional period of MDR & IVDR
  • UK Conformity Assessment (UKCA)
  • Regulatory Updates for Australia
    • MDSAP Changes in regard to Australia jurisdiction
    • Medical devices reforms: Mutual Recognition Agreements
  • Q& A session

About the speaker

Robert Froehlich

Mr. Robert Froehlich
AVP and Head of Medical & Health Services Certification, TÜV SÜD ASEAN

Robert joined TÜV SÜD in 2017 and have since held multiple roles and responsibilities to support the Medical Device industry. He was based out of Germany as a Department Manager – new clients, Senior Product Specialist, Medical Device Lead Auditor and Technical Documentation Assessor. Robert is currently responsible for Medical & Health Service – Certification for ASEAN.


 

Learn more about the Healthcare and Medical Devices services we offer.

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