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Clinical trial protocol
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291	INSTITUTIONAL REVIEW BOARD (IRB) SUBMISSION REQUIREMENTS A. Protocol Preparation. Protocols will be formulated within the mission areas of Coast Guard (CG) or the Department of Homeland Security (DHS). The problem or obj Add to Reading List Source URL: www.uscg.mil Language: English Pharmaceutical sciences Science Food and Drug Administration Pharmacology Drug safety Clinical research coordinator Institutional review board Clinical trial Investigational New Drug Clinical research Research Pharmaceutical industry
292	ClinicalTrials.gov Webinar Series, March 2011 Participant Flow Module Rebecca J. Williams, Pharm.D., M.P.H., Assistant Director, ClinicalTrials.gov National Library of Medicine This presentation will be covering the fir Add to Reading List Source URL: prsinfo.clinicaltrials.gov Language: English - Date: 2014-03-11 16:44:01 Pharmaceutical industry Science Pharmacology ClinicalTrials.gov Clinical trial Trials Communications protocol Modularity Web conferencing Research Clinical trials Clinical research
293	Clinical Interventional Study Protocol Template PREFACE The Clinical Intervention Study Protocol Template is a suggested format for clinical trials sponsored by the National Institute on Aging (NIA). Investigators are e Add to Reading List Source URL: www.nia.nih.gov Language: English - Date: 2014-04-21 12:17:34 Design of experiments Epidemiology Scientific method Pharmacology Evaluation methods Clinical trial Crossover study Data monitoring committees Randomized controlled trial Clinical research Research Science
294	Guidance for Industry Special Protocol Assessment U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER) Add to Reading List Source URL: www.fda.gov Language: English Clinical research FDA Special Protocol Assessment Prescription Drug User Fee Act Center for Biologics Evaluation and Research Clinical trial New Drug Application Center for Drug Evaluation and Research Communications protocol Regulatory requirement Food and Drug Administration Pharmaceutical sciences Health
295	Appendix[removed]: Protocol and Protocol Amendments (MA[removed]) Add to Reading List Source URL: www.fda.gov Language: English Design of experiments Pharmacology Drug safety Institutional review board Clinical trial Lip enhancement Restylane Investigational New Drug Medicis Pharmaceutical Medicine Clinical research Pharmaceutical industry
296	Centers for Medicare & Medicaid Services Research Study Protocol If your study protocol has received federal approval, you may submit the Research Methods section of your proposal in lieu of this Study Protocol. Add to Reading List Source URL: www.resdac.org Language: English - Date: 2013-10-01 10:51:22** Health Science Medicare Form Medicaid Clinical trial Click consonant Research Federal assistance in the United States Healthcare reform in the United States Presidency of Lyndon B. Johnson
297	SOP Table of Contents SOP# version Title Add to Reading List Source URL: www.aihealthsolutions.ca Language: English - Date: 2014-04-09 15:55:54 Pharmaceutics Science Clinical Data Management Food and Drug Administration Standard operating procedure Clinical trial Sop Protocol Clinical research Pharmaceutical industry Research
298	PROTOCOL REVIEW Jerald Silverman, DVM, Column Coordinator Getting around late protocol renewals Add to Reading List Source URL: grants.nih.gov Language: English - Date: 2008-06-06 14:02:09 Animal rights Institutional Animal Care and Use Committee Medical research Office of Laboratory Animal Welfare Grant Protocol Clinical trial Science Scientific method Animal testing
299	Identifying Programs That Impact Teen Pregnancy, Sexually Transmitted Infections, and Associated Sexual Risk Behaviors Review Protocol Version 1.0 Review Authors Add to Reading List Source URL: www.hhs.gov Language: English - Date: 2014-05-01 08:49:40 Scientific method Quasi-experiment Randomized controlled trial Sex education Design of quasi-experiments Random assignment Evidence-based medicine Clinical study design Wraparound Design of experiments Statistics Science
300	EXCOR® Pediatric VAD Post Approval Study Protocol Sponsor: Berlin Heart, Inc 200 Valleywood Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical industry Pharmaceutical sciences Pharmacology Implants Interventional cardiology Ventricular assist device Investigational Device Exemption Clinical trial Adverse event Medicine Health Clinical research

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