RAPS

GHTF Releases Adverse Event Report Standard for Pre-Clinical Trials

The Global Harmonization Task Force (GHTF), a global regulatory body whose duties are set to be assumed shortly by the International Medical Device Regulators Forum (IMDRF), has released a final ...
RAPS

GHTF Releases Guidance on Adverse Event Data Reporting Standard

The Global Harmonization Task Force (GHTF), a global regulatory body whose duties are set to be assumed shortly by the International Medical Device Regulators Forum (IMDRF), has released a final ...