GUIDELINE FOR GOOD CLINICAL PRACTICE

First Page		Document Content
Date: 2012-06-22 05:13:23 Pharmaceutical sciences Pharmaceutics Pharmaceuticals policy Drug safety Clinical trial Good Clinical Practice Institutional review board International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Regulatory requirement Clinical research Research Pharmaceutical industry		GUIDELINE FOR GOOD CLINICAL PRACTICE Add to Reading List Source URL: www.ich.org Download Document from Source Website File Size: 380,04 KB Share Document on Facebook

	INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE Final Concept Paper Q8: Pharmaceutical Development dated 19 September 2003 Endorsed by the ICH SC on 8 DocID: 1m1gQ - View Document
	INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE ICH HARMONISED TRIPARTITE GUIDELINE PHARMACEUTICAL DEVELOPMENT DocID: 1lq6l - View Document
	ICH eCTD Specification Change Control V1.8 INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE DocID: 1gxVi - View Document
	ICH eCTD Specification V 3.2 February 04, 2004 INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE DocID: 1fsNq - View Document
	Federal Register / Vol. 80, NoMonday, May 18, Notices cooperative agreement with the U.S. Department of Education, Rehabilitation DocID: 19XWO - View Document