Call for Comments on the Proposed Document 'Creation and Placement of Unique Device Identifier'

Submitted by admin on Tue, 08/20/2024 - 14:10

For your kind perusal, please find attached the WG9 Proposed Document  'Creation and Placement of Unique Device Identifier'.

Kindly send your comments with the template attached to the GHWP Secretariat (secretariat@ghwp.info) on or before 18 October 2024 (Friday) 12:00noon (GMT+8). Thank you.

Call for Comments on the Proposed Document 'Guidelines for Adverse Event Reporting of Percutaneous Coronary Intervention (PCI) devices for the Medical Device Manufacturer or its Authorized Representative'

Submitted by admin on Fri, 08/02/2024 - 14:37

For your kind perusal, please find attached the WG4 Proposed Document 'Guidelines for Adverse Event Reporting of Percutaneous Coronary Intervention (PCI) devices for the Medical Device Manufacturer or its Authorized Representative'.

Call for Comments on the Proposed Document 'Adverse Event Reporting Guidance for the Medical Device Manufacturer or its Authorized Representative'

Submitted by admin on Fri, 08/02/2024 - 14:29

For your kind perusal, please find attached the WG4 Proposed Document 'Adverse Event Reporting Guidance for the Medical Device Manufacturer or its Authorized Representative'.

Sponsorship opportunities of the 28th GHWP Annual Meeting & GHWP Technical Committee Meeting are now open

Submitted by admin on Mon, 07/29/2024 - 13:23

We are pleased to announce that the sponsorship opportunities for the 28th GHWP Annual Meeting & GHWP Technical Committee Meeting (to be held 9-12 December 2024 in Kuala Lumpur, Malaysia) are now open. Please refer to the attached document for more information about the sponsorship package. 

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