Structured Product Labeling - PDFSEARCH.IO - Document Search Engine

Structured Product Labeling
Results: 235

#	Item
111	National Drug File – Reference Terminology (NDF-RT™) Documentation U.S. Department of Veterans Affairs, Veterans Health Administration December 2010 Version Add to Reading List Source URL: evs.nci.nih.gov Language: English - Date: 2011-03-15 13:44:24 Medicine United States Department of Veterans Affairs Medical informatics Healthcare in the United States Clinical pharmacology Abbreviated New Drug Application Food and Drug Administration Veterans Health Administration Structured Product Labeling Pharmaceutical sciences Pharmacology Health
112	National Drug File – Reference Terminology (NDF-RT™) Documentation U.S. Department of Veterans Affairs, Veterans Health Administration March 2014 Version Add to Reading List Source URL: evs.nci.nih.gov Language: English - Date: 2014-04-02 11:57:41 Pharmaceutical sciences Pharmacology United States Department of Veterans Affairs Healthcare in the United States Structured Product Labeling Food and Drug Administration Abbreviated New Drug Application Veterans Health Administration Unified Medical Language System Health Medicine Medical informatics
113	National Drug File – Reference Terminology (NDF-RT™) Documentation U.S. Department of Veterans Affairs, Veterans Health Administration April 2012 Version Add to Reading List Source URL: evs.nci.nih.gov Language: English - Date: 2012-04-02 10:52:55 Health United States Department of Veterans Affairs Medical informatics Healthcare in the United States Clinical pharmacology Abbreviated New Drug Application Food and Drug Administration Veterans Health Administration Structured Product Labeling Pharmaceutical sciences Pharmacology Medicine
114	DRUG INFORMATION 273 Bioinformatics Modernization and the Critical Path to Improved Benefit-Risk Assessment of Drugs Add to Reading List Source URL: www.fda.gov Language: English Science Clinical research Nursing informatics Standards organizations Medical technology Food and Drug Administration Structured Product Labeling Health Level 7 Bioinformatics Medicine Health Medical informatics
115	FDA Regional Technical Specifications for ICH E2B (R3) Implementation Postmarket Submission of Individual Case Safety Reports (ICSRs) for Vaccines Draft Technical Specifications Document This Document is incorporated by Add to Reading List Source URL: www.fda.gov Language: English Drug safety Research Medical informatics Clinical research Clinical Data Management Vaccine Adverse Event Reporting System Structured Product Labeling Electronic Common Technical Document Adverse Event Reporting System Medicine Health Food and Drug Administration
116	[removed]Federal Register / Vol. 76, No[removed]Monday, May 23, [removed]Notices to have an accredited third party conduct a quality systems regulation inspection of their establishment Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2013-05-23 11:36:41 Medicine Food and drink Pharmaceuticals policy Adulteration United States Public Health Service Federal Food Drug and Cosmetic Act New Drug Application Unique Device Identification Structured Product Labeling Food and Drug Administration Food law Health
117	Microsoft Word - SDSDbackground (3).doc Add to Reading List Source URL: www.fda.gov Language: English Computing Health Level 7 Clinical Document Architecture Clinical Data Interchange Standards Consortium Structured Product Labeling SDTM International HL7 Implementations XForms XML Medical informatics Health Medicine
118	Questions for the Committee Add to Reading List Source URL: www.fda.gov Language: English Medicine Clinical pharmacology Food and Drug Administration Therapeutics United States Public Health Service Labeling theory Structured Product Labeling Pharmaceutical sciences Pharmacology Clinical research
119	PDF Document Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-07-11 14:42:18 Medical informatics Pharmaceutical sciences Pharmaceutical industry Structured Product Labeling Food law New Drug Application Package insert Packaging and labeling Federal Food Drug and Cosmetic Act Medicine Food and Drug Administration Health
120	[removed]Federal Register / Vol. 79, No[removed]Thursday, May 29, [removed]Notices to meet current standards, the Agency will advise ANDA applicants to submit Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-05-29 06:03:01 Technology Premarket approval Medical device Prescription Drug User Fee Act Investigational Device Exemption Structured Product Labeling Unique Device Identification Food and Drug Administration Medicine Health

UPDATE