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 2.

If you have any comments, please send them to the AHWP Secretariat (secretariat@ahwp.info) and copy to the AHWP WG2 Chair, Ms. Jennifer MAK (see1_mdco@dh.gov.hk) and WG2 Co-chair, Dr. SAINI Kulwant (KSAINI@its.jnj.com) on or before 26 Nov 2013.

Thank you.

Download file:Proposed_WG2_1.pdf