For endorsement at the 17th AHWP Meeting in Chinese Taipei - PROPOSED FINAL documents on "Guidelines for Regulatory Auditing of Quality Management Systems of Medical Device Manufacturers (Part 1 - 5)"
After consolidating the comments received from GHWP members by 31 Oct 2012, the PROPOSED document on "Guidelines for Regulatory Auditing of Quality Management Systems of Medical Device Manufacturers (Part 1 - 5)" developed by GHWP WG4 has become the captioned PROPOSED FINAL document, for endorsement at 17th GHWP Meeting in Chinese Taipei.
For endorsement at the 17th AHWP Meeting in Chinese Taipei - PROPOSED FINAL document on "Medical Device Adverse Event (AE) Report Form"
After consolidating the comments received from GHWP members by 31 Oct 2012, the PROPOSED document on "Medical Device Adverse Event (AE) Report Form" developed by GHWP WG2 has become the captioned PROPOSED FINAL document, for endorsement at 17th GHWP Meeting in Chinese Taipei.
Thank you for your notice.
Golden Chance : Last Vacant to Join as AHWP Website Sponsor
The official website of GHWP has been operating through the support of company sponsorship. It is now a golden opportunity for all medical device companies to grasp the last chance to join as a GHWP website sponsor.
AHWP's Participation in ISO / TC 210
ISO / TC 210 has accepted GHWP as a Liaison Member, and invited GHWP to nominate representatives of GHWP to join ISO/TC210 as formal members on behalf of their economies.
AHWP's Participation in the International Medical Device Regulators Forum (IMDRF)
GHWP has accepted the invitation by IMDRF, and confirmed our joining as an IMDRF Affiliated Organization.
In addition, GHWP Chair will represent GHWP at the future IMDRF Management Committee Meetings as an Official Observer.