Capacity Building – Free online training on Medical Device Adverse Event Terminology and General Regulatory Requirements by NMPA, PMDA and SFDA Regulators on 20 November 2024

Submitted by admin on Fri, 11/08/2024 - 08:21

Capacity Building – Free online training on Medical Device Adverse Event Terminology and General Regulatory Requirements by NMPA, PMDA and SFDA Regulators on 20 November 2024

Call for Comments on the Proposed Document 'Guidance Document on Qualification of Medical Device Software'

Submitted by admin on Wed, 10/02/2024 - 23:56

For your kind perusal, please find attached the WG3 Proposed Document 'Guidance Document on Qualification of Medical Device Software'.

Kindly send your comments with the template attached to the GHWP Secretariat (secretariat@ghwp.info) on or before 31 October 2024 (Thursday) 12:00noon (GMT+8). Thank you.

Draft Programme, Sponsorship Opportunities and Registration of GHWP 28th Annual Meeting and 28th GHWP Technical Committee Meeting

Submitted by admin on Thu, 09/26/2024 - 11:13

Draft Programme

Please have the attached DRAFT pragramme (Day 1- Day 4) of GHWP 28th Annual Meeting and 28th GHWP Technical Committee Meeting to be held 9th - 12th December 2024, in Kuala Lumpur of Malaysia.

 

Subscribe to