Federal Register Notice: FDA is making available several proposed and final documents that have been prepared by Study Groups 1, 2, 3, and 4 of the Global Harmonization Task Force (GHTF) on medical devices. These documents are intended to provide information only and represent a harmonized proposal and recommendation from the GHTF Study Groups that may be used by governments developing and updating their regulatory requirements for medical devices. FDA is requesting comments on these documents by 4/25. To view this notice, click here.