CALL FOR COMMENTS on the PROPOSED document "Adverse Event Reporting Timelines Guidance for Medical Device Manufacturer and its Authorised Representative"


                                          
 

The proposed document "Adverse Event Reporting Timelines Guidance for Medical Device Manufacturer and its Authorised Representative”is prepared by AHWP Working Group 2.


If you have any comment, please send them to the AHWP Secretariat (secretariat@ahwp.info) with the template below and copy to the AHWP WG2 Chair, Ms. Jennifer Mak (see1_mdco@dh.gov.hk) and WG2 Acting Co-chair, Ms. Kitty Mao (Kitty.Mao@ge.com) on or before 17 October 2014.

Thank you for your attention.

 

Download file:AHWP-WG2-P001_2014.pdf

 Download file:AHWP Comments Template_verMay2014.docx