Struggling with Technical File and Design Dossier Reviews?

Learn how compiling and maintaining product Technical Files/Design Dossiers in accordance with the European regulatory requirements can be administered while launching safe medical devices into the market in a timely and compliant manner.

LRQA and Medtronic will discuss: 

  • How to effectively collaborate to achieve the common objective
  • How technical documentation is created, managed and submitted from the manufacturer’s standpoint
  • An assessor’s outlook on the evaluation of these dossier

Download "Struggling with Technical File and Design Dossier Reviews?" Webinar now!

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Contact us to learn more about Medical Devices Regulation (MDR)