For endorsement at the 19th AHWP Meeting in Seoul - PROPOSED FINAL document on "Adverse Event Reporting Timelines Guidance for Medical Device Manufacturer and its Authorised Representative"

After consolidating the comments received from GHWP members by 17 Oct 2014, the PROPOSED document on "Adverse Event Reporting Timelines Guidance for Medical Device Manufacturer and its Authorised Representative" developed by GHWP WG4 has become the captured PROPOSED FINAL document, for the endorsement at the 19th GHWP Meeting in Seoul.

Thank you for your notice.

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Adverse Event Reporting Timelines Guidance for Medical Device Manufacturer and its Authorised Representative_PROPOSED FINAL.pdf