Form FDA 483 - PDFSEARCH.IO - Document Search Engine

Form FDA 483
Results: 519

#	Item
331	Generic Drug User Fees Health Leaders Dialogue “PDUFA, MDUFMA & GDUFA: What Lies Ahead” Peter C. Beckerman Senior Policy Advisor FDA Office of Policy, Office of the Commissioner Add to Reading List Source URL: www.fda.gov Language: English Health Pharmacology Pharmaceutical industry Therapeutics United States Public Health Service Prescription Drug User Fee Act Abbreviated New Drug Application Generic drug Form FDA 483 Food and Drug Administration Pharmaceuticals policy Pharmaceutical sciences
332	U.S. CUSTOMS PORT OF ENTRY Form Approved OMB No[removed]Expiration Date: [removed]INSTRUCTIONS 1. If submitting entries electronically through ACS/ABI, hold FDA-2877 in Add to Reading List Source URL: www.customslink.com Language: English - Date: 2011-01-07 21:14:21 Medicine Center for Devices and Radiological Health Abbreviated New Drug Application Form FDA 483 Title 21 CFR Part 11 Food and Drug Administration Pharmaceutical sciences Health
333	FDA’S OVERSIGHT OF NECC AND AMERIDOSE: A HISTORY OF MISSED OPPORTUNITIES? PRELIMINARY MAJORITY STAFF REPORT COMMITTEE ON ENERGY AND COMMERCE U.S. HOUSE OF REPRESENTATIVES Add to Reading List Source URL: energycommerce.house.gov Language: English - Date: 2013-04-16 08:07:33 Pharmaceutical sciences Compounding Form FDA 483 Office of Criminal Investigations Office of Regulatory Affairs Pharmacy Federal Food Drug and Cosmetic Act Center for Drug Evaluation and Research Food and Drug Administration Health Medicine
334	FOOD AND DRUG ADMINISTRATION PROGRAM COMPLIANCE PROGRAM GUIDANCE MANUAL[removed] Add to Reading List Source URL: www.fda.gov Language: English Health Medicine Pharmacology Pharmaceutical industry Drug safety Clinical trial Form FDA 483 Office of Regulatory Affairs Clinical investigator Food and Drug Administration Clinical research Research
335	FOOD AND DRUG ADMINISTRATION COMPLIANCE PROGRAM GUIDANCE MANUAL PROGRAM[removed] Add to Reading List Source URL: www.fda.gov Language: English Technology Premarket approval Center for Devices and Radiological Health Medical device Federal Food Drug and Cosmetic Act Office of Regulatory Affairs Design controls Form FDA 483 Quality management system Food and Drug Administration Medicine Health
336	..”’ . ●,4.8, DEPARTMENT OF HEALTH & HUMAN SERVICES Add to Reading List Source URL: www.fda.gov Language: English** Pharmaceutical sciences Pharmaceutical industry Quality management Quality Form FDA 483 Corrective and preventive action Medical device Government procurement in the United States Quality assurance Medicine Technology Food and Drug Administration
337	Microsoft Word - 1- CP[removed]Coversheet February[removed]Final.doc Add to Reading List Source URL: www.fda.gov Language: English Technology Good manufacturing practice Form FDA 483 Center for Devices and Radiological Health Medical device Design controls Quality management system QSIT Title 21 of the Code of Federal Regulations Food and Drug Administration Medicine Health
338	FDA Oct-Dec2012 Progress Reportv2 Add to Reading List Source URL: www.fda.gov Language: English Medicine Food law Food and drink Adulteration Food Safety Modernization Act Food safety Federal Food Drug and Cosmetic Act Food Safety and Modernization Act Form FDA 483 Food and Drug Administration Pharmaceuticals policy Health
339	U.S. CUSTOMS PORT OF ENTRY Form Approved OMB No[removed]Expiration Date: [removed]INSTRUCTIONS 1. If submitting entries electronically through ACS/ABI, hold FDA-2877 in Add to Reading List Source URL: www.alliancecustoms.com Language: English - Date: 2007-06-08 14:09:43 Medicine Center for Devices and Radiological Health Abbreviated New Drug Application Form FDA 483 Title 21 CFR Part 11 Food and Drug Administration Pharmaceutical sciences Health
340	Consukants $ ::: ,c g f ij rl 12 “(“jf Add to Reading List Source URL: www.fda.gov Language: English - Date: 2001-10-01 16:47:19 Technology Premarket approval Center for Devices and Radiological Health Medical device Title 21 of the Code of Federal Regulations Form FDA 483 Federal Food Drug and Cosmetic Act Food and Drug Administration Medicine Health

UPDATE