After the receipt of comments from members and the review by the GHWP leadership, the Proposed Final Document: Creation and Placement of Unique Device Identifier will be proceeded for endorsement at The GHWP 28th Annual Meeting.
After the receipt of comments from members and the review by the GHWP leadership, the Proposed Final Document: Guidelines on Development of GHWP Documents - Part 2 Structure and Drafting will be proceeded for endorsement at The GHWP 28th Annual Meeting.
After the receipt of comments from members and the review by the GHWP leadership, the Proposed Final Document: Guideline on development of GHWP Documents - Part 1 Procedure for development will be proceeded for endorsement at The GHWP 28th Annual Meeting.
After the receipt of comments from members and the review by the GHWP leadership, the Proposed Final Document: Guidance Document for Medical Device Organizations- Product Localisation for Manufacturing and Importation will be proceeded for endorsement at The GHWP 28th Annual Meet
After the receipt of comments from members and the review by the GHWP leadership, the Proposed Final Document: Comparison study of ISO 13485 vs. QMS requirements in GHWP member countries or regions will be proceeded for endorsement at The GHWP 28th Annual Meeting.
