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Prescription Drug User Fee Act
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31	Federal Register / Vol. 80, No[removed]Tuesday, March 31, [removed]Notices The Food and Drug Administration (FDA) is announcing a request for additional comments on the chemistry, manufacturing, and control (CMC) information Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2015-03-31 08:02:18 Health Investigational New Drug Drug development Regulatory requirement Center for Biologics Evaluation and Research Prescription Drug User Fee Act New Drug Application ClinicalTrials.gov Structured Product Labeling Food and Drug Administration Medicine Pharmaceutical sciences
32	Patient‐Focused Drug Development Public Meeting Public Meeting Theresa M. Mullin, Ph.D. Associate Director for Planning and Informatics FDA Center for Drug Evaluation and Research Add to Reading List Source URL: www.fda.gov Language: English Medicine Pharmacology Pharmaceuticals policy Prescription Drug User Fee Act FDA Fast Track Development Program Fibromyalgia Food and Drug Administration Health Pharmaceutical sciences
33	7616 Federal Register / Vol. 80, No[removed]Wednesday, February 11, [removed]Notices DEPARTMENT OF HEALTH AND HUMAN SERVICES Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2015-02-11 10:21:40 Health Pharmaceutical sciences Prescription Drug User Fee Act Medical device Orphan drug Food and Drug Administration Medicine Pharmaceuticals policy
34	Capital Reporting Company FDA -- Meta-Analysis Guidance[removed]1 CENTER FOR DRUG EVALUATION AND RESEARCH (CDER) Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Center for Drug Evaluation and Research Prescription Drug User Fee Act Center for Biologics Evaluation and Research Food and Drug Administration Medicine Health
35	FY 2015 FDA Operating Plan Add to Reading List Source URL: www.fda.gov Language: English Medicine Pharmaceuticals policy Food and Drug Administration Clinical pharmacology Drugs Prescription Drug User Fee Act Biosimilar Prescription medication Pharmacy Pharmaceutical sciences Health Pharmacology
36	Microsoft Word - 16618dft.doc Add to Reading List Source URL: www.fda.gov Language: English Health Prescription Drug User Fee Act Center for Biologics Evaluation and Research Biosimilar FDA Special Protocol Assessment New Drug Application Generic drug Center for Drug Evaluation and Research Biologic Food and Drug Administration Pharmaceutical sciences Medicine
37	Microsoft Word[removed]doc Add to Reading List Source URL: www.fda.gov Language: English Health Clinical research Pharmacology Pharmaceutical industry Drug safety Prescription Drug User Fee Act Center for Drug Evaluation and Research Investigational New Drug Clinical trial Food and Drug Administration Pharmaceutical sciences Research
38	[removed]Federal Register / Vol. 69, No[removed]Tuesday, September 28, [removed]Notices ‘‘Guidance for Industry: Animal Drug Sponsor Fees Under the Animal Drug Add to Reading List Source URL: www.fda.gov Language: English Pharmaceuticals policy Food law Prescription Drug User Fee Act Center for Biologics Evaluation and Research Medical device Federal Food Drug and Cosmetic Act Food and Drug Administration Medicine Health
39	Non-Clinical Cardiovascular Safety Testing: Moving Forward Add to Reading List Source URL: www.fda.gov Language: English Clinical research Pharmaceutical industry Pharmaceuticals policy Therapeutics Prescription Drug User Fee Act Drug development Center for Drug Evaluation and Research Grepafloxacin Food and Drug Administration Pharmaceutical sciences Pharmacology
40	Overview of FDA Support for Innovation Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Pharmaceuticals policy Clinical research Pharmaceutical industry Therapeutics Prescription Drug User Fee Act Traumatic brain injury Abbreviated New Drug Application Approved drug Medicine Health Food and Drug Administration