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