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User review
Results: 639

#	Item
581	Document Generation System (DGS) Doc Review User Guide[removed] NIH OD OAMP 1. Add to Reading List Source URL: oamp.od.nih.gov Language: English - Date: 2014-01-20 19:07:02 Data compression Proprietary software WinZip File managers Windows Explorer Zip Folder Computer file Computer icon Software System software Computing
582	Guidance for Review Staff and Industry Good Review Management Principles and Practices for PDUFA Products Add to Reading List Source URL: www.fda.gov Language: English Pharmaceuticals policy Pharmaceutical sciences Pharmaceutical industry Drug safety Pharmacology Prescription Drug User Fee Act FDA Special Protocol Assessment Center for Biologics Evaluation and Research New Drug Application Food and Drug Administration Medicine Health
583	Survey of the Presentation of Sex Analysis in the FDA Review of Efficacy and Safety Clinical Data of New Molecular Entity Drugs and Biologics Approved From 2007 to 2009 Onyeka Otugo1, Rita Poon1, Vanessa Copeland1, Kesha Add to Reading List Source URL: www.fda.gov Language: English Research Food and Drug Administration Pharmacology New Drug Application Milnacipran Clinical trial Approved drug FDA Special Protocol Assessment Prescription Drug User Fee Act Pharmaceutical sciences Clinical research Pharmaceutical industry
584	CDER 21st Century Review Desk Reference Guide Add to Reading List Source URL: www.fda.gov Language: English Health Prescription Drug User Fee Act New Drug Application Center for Drug Evaluation and Research Food and Drug Administration Pharmaceutical sciences Pharmacology
585	CDER New Drug Review: 2011 Update Add to Reading List Source URL: www.fda.gov Language: English Medicinal chemistry Clinical pharmacology Pharmaceuticals policy Prescription Drug User Fee Act Pharmaceutical industry Center for Drug Evaluation and Research Drug discovery FDA Special Protocol Assessment Pharmaceutical sciences Food and Drug Administration Pharmacology
586	MANUAL OF POLICIES AND PROCEDURES CENTER FOR DRUG EVALUATION AND RESEARCH MAPP[removed]REVIEW MANAGEMENT Add to Reading List Source URL: www.fda.gov Language: English Research Pharmacology Clinical research Pharmaceutical industry Drug safety Investigational New Drug Clinical trial Prescription Drug User Fee Act New Drug Application Food and Drug Administration Medicine Health
587	NDAs/BLAs: Using the 21st Century Review Process Desk Reference Guide Add to Reading List Source URL: www.fda.gov Language: English Health Prescription Drug User Fee Act New Drug Application Center for Drug Evaluation and Research Food and Drug Administration Pharmaceutical sciences Pharmacology
588	FDASIA Small Business Report Add to Reading List Source URL: www.fda.gov Language: English Health Pharmaceutical sciences Prescription Drug User Fee Act Priority review voucher New Drug Application Federal Food Drug and Cosmetic Act Pharmaceutical industry Center for Devices and Radiological Health Generic drug Food and Drug Administration Medicine Pharmaceuticals policy
589	II. Rights and the functioning of the Single Market II.A Why is it not possible to access many online content services from anywhere in Europe? Question 1: [In particular if you are an end user/consumer:] Have you faced Add to Reading List Source URL: wiki.creativecommons.org Language: English - Date: 2014-03-06 11:27:44 Copyright law of the United States Copyright Limitations and exceptions to copyright Fair use Public domain Fair dealing Copyright law of the European Union Hargreaves Review of Intellectual Property and Growth Law Copyright law Intellectual property law
590	22 April 2010 Strengthening User Engagement – Open Meeting A meeting to discuss the interim findings of a review by the UK Statistics Authority will be held on Thursday 3 June 2010, from 10:00am to 12:30pm at the Royal Add to Reading List Source URL: www.statisticsauthority.gov.uk Language: English Email Technology Digital media

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