MDR Flowchart Explains When Legacy Devices Can Benefit From Extended Timelines
Are you uncertain whether your medtech products can benefit from transition period extensions that feature in the March 2023 amending Regulation to the MDR? The latest European Commission document offers help.
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The European Commission has provided an early revision of a critical Q&A document to help manufacturers better understand how to keep legacy products on the EU market.
The deadlines for legacy products under the Medical Device Regulation have changed. Here are the essentials that all medtech players need to understand in how the MDR has now been amended.
The EU notified body association, TEAM-NB, is working hard to support industry with its MDR and IVDR compliance efforts. Its first technical documentation training session highlighted where help is likely to be most needed.