GHTF Releases Proposed Guidance on Medical Device STEDs
The Global Harmonization Task Force’s (GHTF) Study Group 1 has issued new guidance for regulatory authorities, conformity assessment bodies and the device industry on the documentation of evidence necessary to show conformity to regulatory requirements.
300 N. Washington St., Suite 200, Falls Church, VA 22046, USA.
Phone (703) 538-7600 - Fax (703) 538-7676 - Toll free (888) 838-5578.
Copyright by FDAnews. All rights reserved. Do not duplicate or redistribute in any form.