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User review
Results: 639

#	Item
371	CLINICAL REVIEW Application Type Submission Number Submission Code Letter Date Add to Reading List Source URL: www.fda.gov Language: English Chemistry Didanosine Pharmacology Reverse-transcriptase inhibitor Prescription Drug User Fee Act Abacavir Videx Tenofovir Norfloxacin Purines Bristol-Myers Squibb Organic chemistry
372	Prescription Drug User Fee Act (PDUFA) Webinar 1 Add to Reading List Source URL: www.fda.gov Language: English Medicine Prescription Drug User Fee Act Pharmaceutical sciences FDA Special Protocol Assessment Abbreviated New Drug Application Center for Drug Evaluation and Research Center for Biologics Evaluation and Research Priority review voucher Food and Drug Administration Pharmaceuticals policy Health
373	FDA Drug Review in PDUFA IV John K. Jenkins, MD Director, Office of New Drugs (CDER) 1 Add to Reading List Source URL: www.fda.gov Language: English Clinical research Health Pharmacology Therapeutics United States Public Health Service Prescription Drug User Fee Act Prison Rape Elimination Act Food and Drug Administration Amendments Act Pharmaceutical sciences Food and Drug Administration Pharmaceuticals policy
374	Microsoft Word - PDUFA V Committment Letter[removed]docx Add to Reading List Source URL: www.fda.gov. Language: English Prescription Drug User Fee Act Health New Drug Application FDA Special Protocol Assessment Priority review voucher Food and Drug Administration Pharmaceutical sciences Pharmacology
375	[NOTE TO USER: THE INSTRUCTIONS IN THIS DOCUMENT BETWEEN BRACKETS – [ Add to Reading List Source URL: www.civillawselfhelpcenter.org Language: English - Date: 2013-08-15 15:28:48 Petitioner Law Thomas v. Review Board of the Indiana Employment Security Division
376	Outfitter / User / Agency Meeting Agenda January 26, [removed]:00 a.m. PST Human Waste in the Rogue River Canyon • Review proposed Wild Rogue River Human Waste Removal System (HWRS) language • Review Portable Toilet Gu Add to Reading List Source URL: www.blm.gov - Date: 2012-01-11 11:19:31
377	NDAs and BLAs: Communication to Applicants of Planned Review Timelines Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Prescription Drug User Fee Act Federal Food Drug and Cosmetic Act New Drug Application Center for Drug Evaluation and Research FDA Fast Track Development Program Food and Drug Administration Medicine Health
378	SOPP[removed]: Scheduling and Conduct of Regulatory Review Meetings with Sponsors and Applicants Version #5 Effective Date: October 15, 2012 I. Purpose Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences FDA Special Protocol Assessment Prescription Drug User Fee Act New Drug Application FDA Fast Track Development Program Center for Biologics Evaluation and Research Meeting Investigational New Drug Validation Food and Drug Administration Medicine Health
379	st 21 Century Review Judit Milstein Add to Reading List Source URL: www.fda.gov Language: English Prescription Drug User Fee Act Pharmacology Health Drug safety Patent law New Drug Application Priority right Food and Drug Administration Pharmaceutical sciences Pharmaceuticals policy
380	st 21 Century Review Judit Milstein Add to Reading List Source URL: www.fda.gov Language: English Prescription Drug User Fee Act Pharmacology Health Drug safety Patent law New Drug Application Priority right Food and Drug Administration Pharmaceutical sciences Pharmaceuticals policy

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