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Monitoring in clinical trials
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41	Clinical Trial Consent Form Template STUDY TITLE: The full study title should be placed here. An abbreviated study title that is more understandable to the subject may be used. Add to Reading List Source URL: www.gasha.nshealth.ca Language: English - Date: 2013-06-12 11:17:12 Pharmaceutical sciences Pharmaceutical industry Design of experiments Evaluation methods Clinical trial Food and Drug Administration Clinical research coordinator Monitoring in clinical trials Research Clinical research Pharmacology
42	This document is intended for the use of the DCP Consortia staff conducting cancer chemoprevention studies under contract with the NCI/DCP. ________________________________________________________________________________ Add to Reading List Source URL: prevention.cancer.gov Language: English - Date: 2014-09-10 13:27:00 Science Pharmaceutics Clinical trial Clinical research associate Standard operating procedure Monitoring in clinical trials Clinical research Pharmaceutical industry Research
43	Monitoring Bone Toxicity in Pediatric Clinical Trials of Tenofovir Disoproxil Fumarate Linda L. Lewis, M.D. Medical Team Leader Division of Antiviral Products, CDER Add to Reading List Source URL: www.fda.gov Language: English Microbicides Purines Tenofovir Antiretroviral drug Dual-energy X-ray absorptiometry Bone density Biomarker Osteocalcin Bone Medicine Biology Chemical pathology
44	Microsoft Word - OCC CRA Hearing Aug[removed]doc Add to Reading List Source URL: www.occ.gov Language: English - Date: 2010-09-08 15:18:48 Community Reinvestment Act United States housing bubble Economy of the United States Wells Fargo Banking in the United States Dodd–Frank Wall Street Reform and Consumer Protection Act Government policies and the subprime mortgage crisis Monitoring in clinical trials United States federal banking legislation Mortgage industry of the United States Politics of the United States
45	Guidelines for Developing a Monitoring Plan Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2011-10-18 14:24:00 Pharmaceutical sciences Pharmaceutical industry Pharmacology Drug safety Design of experiments Data monitoring committees Clinical trial Monitoring in clinical trials Pharmacovigilance Clinical research Research Medicine
46	Guide for Developing a Monitoring Plan for Studies Sponsored by NIAMS Last Revised[removed] Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2011-10-18 14:23:26 Pharmaceutical sciences Pharmaceutical industry Pharmacology Drug safety Design of experiments Data monitoring committees Clinical trial Monitoring in clinical trials Pharmacovigilance Clinical research Research Medicine
47	This document is intended for the use of the DCP Consortia staff conducting cancer chemoprevention studies under contract with the NCI/DCP. ________________________________________________________________________________ Add to Reading List Source URL: prevention.cancer.gov Language: English - Date: 2013-06-27 17:24:30 Research Health Clinical trial Good Clinical Practice Medical guideline Monitoring in clinical trials Pharmaceutical industry Clinical research Medicine
48	DRAFT DRAFT DRAFT DRAFT DRAFT DRAFT DRAFT DRAFT Add to Reading List Source URL: www.tn.gov Language: English - Date: 2012-05-16 16:29:26 Government procurement in the United States Administration of federal assistance in the United States OMB A-133 Compliance Supplement Monitoring in clinical trials Single Audit United States Office of Management and Budget Compliance requirements
49	DCP CONSORTIA 2012 STANDARD OPERATING PROCEDURES SOP 12: CLO Monitor Instructions for Conducting Monitoring Visits Add to Reading List Source URL: prevention.cancer.gov Language: English - Date: 2014-09-04 12:23:43 Medical ethics Hospice Nursing Patient safety Case report form Monitoring in clinical trials Medicine clinical research Health
50	DCP CONSORTIA 2012 STANDARD OPERATING PROCEDURES SOP 11: CLO Monitor Qualifications Add to Reading List Source URL: prevention.cancer.gov Language: English - Date: 2014-09-04 12:21:21 Science Knowledge Clinical trial Standard operating procedure Clinical research associate Protocol Monitoring in clinical trials Clinical research Pharmaceutical industry Research

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