China: SFDA Draft Aims to Bolster Quality of Device Clinical Trials
China’s proposed update to good clinical practice requirements for medical devices includes tougher provisions on ethics committees and human subject protections.
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.