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Monitoring in clinical trials
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31	DRAFT DRAFT DRAFT DRAFT DRAFT DRAFT DRAFT DRAFT Add to Reading List Source URL: www.state.tn.us 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
32	Dr. Nuon Sarith pauses for a moment while caring for AIDS patients in Phnom Penh, Cambodia. 68 Communications Handbook for Clinical Trials Jim Daniels Add to Reading List Source URL: www.fhi360.org Language: English - Date: 2014-06-05 14:16:25 Nursing research Medicine Pharmaceutical industry Crisis Crisis management Management Clinical trial Data monitoring committees National Institutes of Health Research Clinical research Health
33	The Clinical Investigator: Responsibilities in Medical Device Clinical Trials Presented by Catherine Parker, RN Consumer Safety Officer Division of Bioresearch Monitoring Add to Reading List Source URL: www.fda.gov. Language: English Research Health Food and Drug Administration Design of experiments Pharmaceutical industry Clinical trial Institutional review board Clinical investigator Center for Devices and Radiological Health Medicine Pharmacology Clinical research
34	The Sponsor: Responsibilities in Medical Device Clinical Trials Presented by Catherine Parker, RN Consumer Safety Officer Division of Bioresearch Monitoring Add to Reading List Source URL: www.fda.gov. Language: English Clinical research Pharmaceutical industry Food and Drug Administration Design of experiments Clinical trial Pharmaceutical sciences Pharmacology Research
35	State of Vermont Monitoring Strategies A Guidebook for AOT Grantees on Subrecipient Oversight CKrauss Add to Reading List Source URL: vtransgrants.vermont.gov Language: English - Date: 2013-06-07 08:59:19 pharmaceutical industry Information technology management Monitoring in clinical trials clinical research
36	Guide for Developing a Monitoring Plan for Studies Sponsored by NIAMS Last Revised[removed] Add to Reading List Source URL: 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
37	Guidelines for Developing a Monitoring Plan Add to Reading List Source URL: 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
38	State of Vermont Monitoring Strategies A Guidebook for AOT Grantees on Subrecipient Oversight CKrauss Add to Reading List Source URL: vtransgrants.vermont.gov Language: English - Date: 2013-06-10 10:45:56 pharmaceutical industry Information technology management Monitoring in clinical trials clinical research
39	Audience Questions from Oct. 24 Guidance Webinar Oversight of Clinical Investigations -- A Risk-Based Approach to Monitoring Add to Reading List Source URL: www.fda.gov. Language: English Pharmacology Pharmaceutical industry Food and Drug Administration United States Public Health Service Clinical site Monitoring in clinical trials Clinical trial Clinical research Pharmaceutical sciences Research
40	Clinical Trial Quality and Compliance: An FDA Perspective Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 04:07:42 Pharmacology Science Pharmaceutical industry Scientific method Food and Drug Administration Clinical trial Institutional review board Clinical research coordinator Monitoring in clinical trials Clinical research Research Design of experiments

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