The proposed document "Quality Management System-Medical Devices Requirements for Distributors, Importers and Authorized Representative" is prepared by GHWP Working Group 7.

If you have any comments, please send them to the GHWP Secretariat (secretariat@ahwp.info) with the template below and copy to the GHWP WG7 Chair, Mr. Aidahwaty M. Olaybal (aidahwaty@mdb.gov.hk) and WG7 Co-chair, Mr. Ee Bin LIEW (peace_within@hotmail.com) on or before 24 Nov 2016.

Thank you for your attention.