MHRA - Draft guidance on specific device vigilance reporting

bio_subbu

bio_subbu

Super Moderator
Dear All

The MHRA has recently published in its website two draft guidance documents on implementation of the EU vigilance system for specific device types - breast implants and neurostimulators.

1. Draft guidance on the vigilance system for CE-marked medical devices – Breast Implants

2. Draft guidance on the vigilance system for CE-marked medical devices – Neurostimulators

Regards
S. Subramaniam
 
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