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)"

Submitted by admin on Thu, 11/01/2012 - 14:37


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 "Definition and Classification of Field Corrective Actions, including Field Safety Corrective Actions, Recalls and Non Safety related Field Corrective Actions"

Submitted by admin on Thu, 11/01/2012 - 14:20

For endorsement at the 17th AHWP Meeting in Chinese Taipei - PROPOSED FINAL document on "Medical Device Adverse Event (AE) Report Form"

Submitted by admin on Thu, 11/01/2012 - 14:15


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.

Subscribe to