News European Union New medtech regulations Newsletter Transition Periods

Recommendations on the use of Guidance Documents

Posted on 07.07.2022

MedTech Europe and its members recently published a position paper providing the sector’s view on how to use guidance documents without disrupting manufacturers’ efforts to transition to the new rules of the MDR and IVDR.

Please follow this link to access the document.

For more information, please contact Merlin Rietschel, Senior Manager Medical Devices.