The International Medical Device Regulators Forum (IMDRF) has been really busy of late, which is a good thing as many in the medical device industry are still wondering if the IMDRF will live up to the “Big Shoes” that the
GHTF has transitioned to IMDRF
As of November 2012 the GHTF (Global Harmonization Task Force) is no longer operating as evidenced by several pieces of information. In it’s place the International Medical Device Regulators Forum (IMDRF) is working to “build on the strong foundation of
GHTF Just Released New & Updated Documents
The Global Harmonization Task Force (GHTF) recently had a meeting and with that came a slew of final documents that were issued on 2 Nov 2012.
GHTF to morph into Int’l Med Dvc Regulators’ Forum (IMDRF)
The GHTF has been around for almost 20 years and is in the process of disbanding to become a more Regultor focused group called the International Medical Device Regulators’ Forum (IMDRF). In the Eucomed 18 Nov 2011 newsletter article they
GHTF Proposal for Unique Device Identification (UDI) System for Medical Devices
The Global Harmonization Task Force Ad Hoc Working Group has drafted a proposal for Unique Device Indentification (UDI). The document is GHTF/AH/(PD2)N2R2 and can be accessed by clicking here. The document was posted on 22 Nov 2010 and comments are