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Orphan Drug Act
Results: 190

#	Item
141	Office of Orphan Products Development FY 2004 Actual FY 2005 Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Food and Drug Administration Drug discovery Epidemiology Pharmaceuticals policy Orphan drug Orphan Drug Act Clinical trial Rare disease Medicine Pharmaceutical sciences Health
142	The FDA’s Office of Orphan Products Development (OOPD) is responsible for regulating orphan products under the Orphan Drugs Act Add to Reading List Source URL: www.fda.gov Language: English Health Pharmaceutical sciences Pharmacology Food and Drug Administration Clinical trial Clinical investigator Institutional review board Investigational New Drug Safety monitoring Research Clinical research Pharmaceutical industry
143	The FDA’s Office of Orphan Products Development (OOPD) is responsible for regulating orphan products under the Orphan Drugs Act Add to Reading List Source URL: www.fda.gov Language: English Medicine Pharmacology Pharmaceutical industry Clinical investigator Institutional review board Investigational New Drug Food and Drug Administration Safety monitoring Regulatory requirement clinical research Research Health
144	Overview of the FDA and the Office of Orphan Products Development (OOPD) Add to Reading List Source URL: www.fda.gov Language: English Pharmaceuticals policy Adulteration Food law Clinical research Federal Food Drug and Cosmetic Act Elixir sulfanilamide Frances Oldham Kelsey Premarket approval Medical device Medicine Food and Drug Administration Health
145	Welcoming Address: “Do an Orphan Designation” Workshop Add to Reading List Source URL: www.fda.gov Language: English Pharmaceuticals policy Clinical research Pharmacology Drug discovery Orphan drug Orphan Drug Act Prescription Drug User Fee Act Clinical trial FDA Fast Track Development Program Pharmaceutical sciences Food and Drug Administration Health
146	Orphan Drug Designation Identifier Add to Reading List Source URL: www.fda.gov Language: English Pharmaceuticals policy Clinical pharmacology Pharmaceutical industry Orphan drug Orphan Drug Act Abbreviated New Drug Application Food and Drug Administration Rare disease Drug discovery Pharmaceutical sciences Pharmacology Health
147	Department of Health and Human Services Food and Drug Administration COMMON EMEA / FDA APPLICATION FOR ORPHAN MEDICINAL PRODUCT DESIGNATION Add to Reading List Source URL: www.fda.gov Language: English Pharmaceuticals policy Food and Drug Administration Pharmaceutical industry Clinical research United States Public Health Service European Medicines Agency Orphan drug Federal Food Drug and Cosmetic Act Drug Master File Pharmaceutical sciences Health Pharmacology
148	Developing Your Orphan Drug Marlene E. Haffner, M.D., M.P.H. Director, FDA Office of Orphan Products Development Add to Reading List Source URL: www.fda.gov Language: English Pharmaceuticals policy Pharmacology Drug discovery Orphan drug Food and Drug Administration Orphan Drug Act Rare disease Xyrem Prescription Drug User Fee Act Pharmaceutical sciences Health Clinical research
149	Federal Register / Vol. 79, No[removed]Tuesday, July 8, [removed]Notices strengthen regulatory capacity throughout the Americas in ways that provide benefit and contribution to the FDA regulatory and public health mission. Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-07-08 00:12:47 Health Clinical research Pharmacology Clinical pharmacology United States Public Health Service Prescription Drug User Fee Act Norfloxacin Orphan drug Unique Device Identification Pharmaceuticals policy Food and Drug Administration Pharmaceutical sciences
150	LYN14091 S.L.C. 113TH CONGRESS 2D SESSION Add to Reading List Source URL: rarediseaseday.us Language: English - Date: 2014-03-04 16:17:18 Pharmaceuticals policy Epidemiology Rare Disease Day Orphan drug Orphan Drug Act National Organization for Rare Disorders Cystic fibrosis Genetic disorder National Institutes of Health Health Medicine Rare diseases