PDUFA IV IT PLAN ABBREVIATED UPDATE MAY 2010

First Page		Document Content
Pharmaceutical sciences Medicine Prescription Drug User Fee Act Electronic Common Technical Document Regulated Product Submissions Food and Drug Administration Pharmaceuticals policy Health		PDUFA IV IT PLAN ABBREVIATED UPDATE MAY 2010 Add to Reading List Source URL: www.fda.gov Download Document from Source Website File Size: 590,82 KB Share Document on Facebook

	Regulated Product Submissions (RPS) Nancy Shadeed DITTA Workshop on RPS March 23, 2015 DocID: 1eXev - View Document
	IMDRF Table of Contents (ToC) Pilot Plan DocID: 11D6b - View Document
	IMDRF/RPS WG/N26FINAL:2015 DocID: W7Sv - View Document
	Proposed document: Assembly and Technical Guide for IMDRF Table of Contents (ToC) Submissions (ToC-based submissions) DocID: W45m - View Document
	How FDA validates reported suspect products in adverse event reports submitted to FAERS DocID: JP2X - View Document