Medical Appliances Committee, Laboratory Materials’ Committee, Pharmaceutical Company Registration Committee and Price Determination Committee. The most important …

The WHO Collaborative Registration Procedure (CRP) is a reliance and collaboration mechanism to facilitate and accelerate the assessment and registration of medical products in participating …

Progress towards enhancing regulatory practices related to medical products around the world is supported by capacity building, promoting regulatory convergence and harmonization.

Nov 14, 2024 · Collect feedback and recommendations to enhance CRP processes for NRAs, SRAs, manufacturers, and stakeholders. Discuss strategies to optimize national registration …

ASEAN, an economic grouping of 10 countries in Southeast Asia has set up a committee responsible for MD regulatory harmonization - The Medical Device Product Working Group …

The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) is an initiative that brings together regulatory authorities and pharmaceutical …

Good Registration Management (GRM) is a concept to promote efficient registration process for medical products by promoting Good Review Practice (GRevP) and Good Submission …

The Gulf Centralised Committee for Drug Registration (GCC-DR), as part of the Gulf Health Council (GHC), enables the consolidated registration of pharmaceutical products throughout …

Dec 30, 2024 · DEPARTMENT OF HEALTH AND HUMAN SERVICES. Food and Drug Administration [Docket No. FDA-2024-N-5720] General and Plastic Surgery Devices Panel of …

Jan 20, 2025 · Professor Richard Reilly is re-appointed to the Health Products Regulatory Authority (HPRA) and as a member and Chairperson of the Advisory Committee for Medical …