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Center for Drug Evaluation and Research
Results: 4314

#	Item
401	Minutes from the May 7-8, 2012 PAC meeting held at the Hilton Rockville Executive Meeting Center Add to Reading List Source URL: www.fda.gov Language: English Influenza Center for Biologics Evaluation and Research Adverse Event Reporting System Center for Drug Evaluation and Research Oseltamivir Flu pandemic Food and Drug Administration Medicine Health
402	DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration Center for Drug Evaluation & Research Office of Translational Sciences Add to Reading List Source URL: www.fda.gov
403	979 W H O Te c h n i c a l Add to Reading List Source URL: www.wsmi.org Language: English - Date: 2013-11-18 07:43:58 Pharmacology Vaccination Influenza vaccine Center for Biologics Evaluation and Research World Health Organization Hepatitis B vaccine Food and Drug Administration Drug reference standard Virus Medicine Health Vaccines
404	Microsoft Word - DRAFT Minutes ver 3 FDA-PhRMA-BIO.doc Add to Reading List Source URL: www.fda.gov Language: English Health Pharmaceutical sciences Prescription Drug User Fee Act Center for Biologics Evaluation and Research Food and Drug Administration Medicine Pharmaceuticals policy
405	DRAFT August 14, 2014 ADVISORY COMMISSION ON CHILDHOOD VACCINES (ACCV) Parklawn Building, 5600 Fishers Lane, Rockville, Maryland Add to Reading List Source URL: www.hrsa.gov Language: English - Date: 2014-12-09 01:13:12 Medicine Health Vaccines Center for Biologics Evaluation and Research Influenza Vaccine Adverse Event Reporting System PM Vaccine injury Drug safety Food and Drug Administration Safety
406	FY 2004 PERFORMANCE REPORT Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Center for Devices and Radiological Health Medical device Center for Biologics Evaluation and Research Biologic Center for Drug Evaluation and Research Federal Food Drug and Cosmetic Act Biosimilar Title 21 of the Code of Federal Regulations Medicine Food and Drug Administration Health
407	Agenda for Quarterly Meeting on MDUFMA / MDUFA Performance January 2012 Welcome. Barbara Zimmerman, CDRH-ODE. Add to Reading List Source URL: www.fda.gov Language: English Center for Biologics Evaluation and Research Center for Devices and Radiological Health Premarket approval Medical device Food and Drug Administration Medicine Health
408	Next-generation Sequencing (NGS) Technology, data formats standardization and promotion of interoperability protocols September 24 & 25, 2014 8:30 am- 5:00 pm Porter Conference Center, Building 35, NIH Campus Add to Reading List Source URL: www.fda.gov Language: English Medicine Pharmaceutical sciences Health Clinical research United States Public Health Service Validation Center for Biologics Evaluation and Research Verification and validation Center for Food Safety and Applied Nutrition Food and Drug Administration Pharmaceutical industry Validity
409	Meeting the Challenges of Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration National Institutes of Health Pharmacology Center for Drug Evaluation and Research Clinical investigator Medicine Health Clinical research
410	Critical Path Innovation Meetings Guidance for Industry DRAFT GUIDANCE This guidance document is being distributed for comment purposes only. Comments and suggestions regarding this draft document should be submitted wit Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Medicine Pharmaceutical industry Clinical pharmacology United States Public Health Service Investigational New Drug Center for Drug Evaluation and Research Drug development Food and Drug Administration Pharmaceutical sciences Clinical research

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