
GHTF final documents - International Medical Device Regulators Forum
The Global Harmonization Task force (GHTF) final documents are still current. As the work of IMDRF progresses, these documents will be reviewed and published as IMDRF documents.
GHTF Archives - International Medical Device Regulators Forum
The International Medical Device Regulators Forum (IMDRF) is continuing the work of the Global Harmonization Task Force (GHTF). GHTF was conceived in 1992 in an effort to achieve greater …
Documents | International Medical Device Regulators Forum
GHTF final documents Final documents created by the Global Harmonization Task force (GHTF) that are still current.
GHTF Mission Summary - International Medical Device Regulators Forum
The Global Harmonization Task Force (GHTF) was a voluntary group of representatives from national medical device regulatory authorities and the regulated industry.
GHTF History | International Medical Device Regulators Forum
These talks would develop into a working framework put forth by the representatives of the European Commission two months later, and would lead to the inaugural meeting of the organisation now …
About IMDRF - International Medical Device Regulators Forum
IMDRF is a voluntary group of medical device regulators from around the world who have come together to build on the strong foundational work of the Global Harmonization Task Force on Medical Devices …
GHTF Organisational Structure - International Medical Device …
The original concept behind the formation of the Global Harmonization Task Force (GHTF) was to bring together experienced regulators and industry members on a regular basis in order to discuss ways in …
GHTF Archived Documents - International Medical Device Regulators …
Historical information and archived documents of the Global Harmonization Task Force on Medical Devices (GHTF).
GHTF Study Group 3 - Quality Systems - International Medical Device ...
Nov 2, 2012 · GHTF Study Group 3 - Quality Systems This page contains final documents produced by the GHTF Study Group 3. For a list of archived documents, see GHTF Archived Documents.
The document herein was produced by the Global Harmonization Task Force, which is comprised of representatives from medical device regulatory agencies and the regulated industry.