CALL FOR COMMENTS on the PROPOSED document "Adverse Event Reporting Guidance for the Medical Device Manufacturer or its Authorized Representative"

 
                                          
 

The proposed document "Adverse Event Reporting Guidance for the Medical Device Manufacturer or its Authorized Representative" is prepared by AHWP Working Group 4.


If you have any comments, please send them to the AHWP Secretariat (secretariat@ahwp.info) with the template below and copy to the AHWP WG4 Chair, Ms Jennifer MAK (see1_mdco@dh.gov.hk) and WG4 Co-chair, Ms. Kitty MAO (kitty.mao@ge.com) on or before 30 Sep 2015.


Thank you for your attention.

 

 

 Download file:AHWP-WG4-AE Reporting_PROPOSED.pdf 

 Download file:AHWP Comments Template_verMay2014.docx