Agenda (Final) for the 17th AHWP Meeting, AHWP TC Meeting and Workshop on 2nd - 6th Nov 2012 in Chinese Taipei
Dear all participants,
Please kindly find the final agenda for your information.
Thank you very much.
Dear all participants,
Please kindly find the final agenda for your information.
Thank you very much.
After consolidating the comments received from GHWP members by 31 Oct 2012, the PROPOSED document on "Amendment 1 to the Global Harmonization Working Party House Rule" developed by GHWP Secretariat has become the captioned PROPOSED FINAL document, for resolution at 17th GHWP Meeting in Chinese Taipei.
Thank you for your notice.
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.
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.
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.
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.
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.