Optimizing your eCTD ANDA

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Pharmaceutical industry Clinical Data Management Medical informatics Drug safety Electronic Common Technical Document International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Drug Master File Abbreviated New Drug Application Food and Drug Administration Clinical research Research Medicine		Optimizing your eCTD ANDA Add to Reading List Source URL: www.fda.gov Download Document from Source Website File Size: 328,82 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