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Clinical trial protocol
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11	Reporting Standards for Social Science Experiments Kevin Esterling University of California - Riverside Summer Institute June 2014 Add to Reading List Source URL: www.bitss.org Language: English - Date: 2016-01-25 14:33:04 Design of experiments Scientific method Experiments Clinical research Statistical methods Blind experiment American Association for Public Opinion Research Protocol Consolidated Standards of Reporting Trials Public Responsibility in Medicine and Research Research Randomized controlled trial
12	ANNEX 2 AF/02-007b/04 Document Receipt Form Protocol Number: Submitted date: Protocol Version Number: Add to Reading List Source URL: www.health.gov.bt Language: English - Date: 2016-06-29 07:05:05 Clinical research Pharmaceutical industry Clinical data management Medical ethics Case report form Clinical trial Informed consent Protocol Email Consent
13	UH eProtocol Investigator User Manual Add to Reading List Source URL: www.fmp.hawaii.edu Language: English - Date: 2016-07-29 16:02:18 Design of experiments Clinical research Pharmaceutical industry Drug safety Institutional review board Clinical trial Communications protocol Email
14	Protocol ID: PD: Meeting Date: Protocol Title: Checklist completed by (IRB Staff name): Date: Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2014-02-06 14:47:15 Medical research Research Medical ethics Design of experiments Health Clinical research Pharmaceutical industry Clinical trial Institutional review board Health Insurance Portability and Accountability Act Health insurance Experiment
15	Proposal for Modernization of CLIA Regulations for Laboratory Developed Testing Procedures (LDPs) Transparency. Quality. Innovation. Desired Outcomes: • Patients receive the most appropriate test(s) for their clinical Add to Reading List Source URL: www.amp.org Language: English - Date: 2015-08-17 17:19:34 Health Medical research Laboratories Clinical Laboratory Improvement Amendments Health in the United States Safety Medical technology Medical laboratory Clinical trial Food and Drug Administration Protocol
16	Zusammenfassung des Studienprotokolls (Synopsis) Die Zusammenfassung stellt ein Kerndokument für die Ethikkommission dar und soll für eine interdisziplinär zusammengesetzte Forschungsethikkommission zwar wissenschaftl Add to Reading List Source URL: www.swissethics.ch Language: English - Date: 2015-07-15 19:15:29 Pharmacology Medicine Evaluation methods Pharmaceutical industry Design of experiments Clinical trial Crossover study Protocol Placebo Clinical research Research Science
17	Microsoft Word - 9124dft.doc Add to Reading List Source URL: www.fda.gov Language: English Design of experiments Clinical research Pharmaceutical industry Pharmacology Clinical trial Interim analysis Clinical study design Drug development FDA Special Protocol Assessment Medical statistics Science Research
18	SOP 17 Data And Safety Monitoring Add to Reading List Source URL: ohsr.od.nih.gov Language: English - Date: 2014-08-14 12:09:35 Medicine Pharmaceutical industry Pharmacology Nursing research Clinical trial National Institutes of Health Data monitoring committees Food and Drug Administration Protocol Research Health Clinical research
19	ISHLT STANDARDS AND GUIDELINES DOCUMENT DEVELOPMENT PROTOCOL TABLE OF CONTENTS I. Documents under Standards and Guidelines (S&G) Committee purview Add to Reading List Source URL: www.ishlt.org Language: English - Date: 2013-01-05 20:19:06 Medical informatics Academic publishing Academic literature Nursing research Medical guideline Web Accessibility Initiative Evidence-based medicine Peer review Clinical trial Medicine Health Science
20	SOP 8 PROCEDURES AND REQUIRED DOCUMENTATION FOR SUBMISSION AND INITIAL REVIEW OF PROTOCOLS Add to Reading List Source URL: ohsr.od.nih.gov Language: English - Date: 2014-03-11 11:22:54 Clinical research National Institutes of Health Design of experiments Pharmacology Nursing research Institutional review board Clinical trial Protocol ClinicalTrials.gov Research Medicine Health

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