Clinical research coordinator - PDFSEARCH.IO - Document Search Engine

Clinical research coordinator
Results: 1108

#	Item
531	Microsoft Word - American University IRB Application Checklist Add to Reading List Source URL: www.american.edu Language: English - Date: 2014-06-30 14:38:20 Pharmaceutical industry Public Responsibility in Medicine and Research Consent Deception Experimentation on prisoners Institutional review board Clinical research coordinator Ethics Clinical research Behavior
532	ADVERSE EVENT REPORTING GUIDELINES CCF Clinical Research Unit-CRU The RSA must be informed of adverse events to assess if the risk: benefit status of the study has changed. In general, an Adverse Event (AE) is any unto Add to Reading List Source URL: www.lerner.ccf.org Language: English - Date: 2014-10-31 14:07:24 Pharmaceutical sciences Pharmaceutics Adverse event Serious adverse event Clinical trial Randomized controlled trial Risk Clinical research coordinator Adverse effect Clinical research Pharmaceutical industry Research
533	Columbia University IRB Guidance for Collaborating Individual Investigators October 29, 2013 This document provides guidance relating to the use of Individual Investigator Agreements to extend the coverage of Columbia Un Add to Reading List Source URL: www.cumc.columbia.edu Language: English - Date: 2013-10-29 16:29:21 Research Drug safety Scientific method Ethics Institutional review board Institute of Internal Auditors Clinical research coordinator Cooperative Human Tissue Network Clinical research Design of experiments Pharmacology
534	COLUMBIA UNIVERSITY INSTITUTIONAL REVIEW BOARD GUIDANCE ON RESEARCH INVOLVING GENETIC TESTING I. SCOPE: This guidance applies to all human subjects research that involves Genetic Testing, as defined below. It provides ba Add to Reading List Source URL: www.cumc.columbia.edu Language: English - Date: 2013-01-08 12:22:12 Health Science Medical genetics Pharmaceutical industry Pharmacology Genetic testing Clinical research coordinator Informed consent Institutional review board Medicine Medical ethics Clinical research
535	Informed Consent Guidelines 1. The consent form must be presented on SIAST letterhead. Photocopied letterhead is acceptable. Add to Reading List Source URL: programs.siast.sk.ca Language: English - Date: 2009-12-10 11:41:08 Medical ethics Research Research ethics Informed consent Human subject research Consent Institutional review board Clinical research coordinator Clinical research Applied ethics Ethics
536	South Carolina Department of Mental Health Add to Reading List Source URL: www.state.sc.us Language: English - Date: 2012-05-29 13:42:28 Science Medical ethics Design of experiments Pharmacology Pharmaceutical industry Institutional review board Clinical trial Clinical research coordinator Informed consent Clinical research Ethics Research
537	EXPEDITED REVIEW OF MINOR CHANGES IN A PREVIOUSLY Add to Reading List Source URL: www.research.uky.edu Language: English - Date: 2008-03-17 10:05:47 Health Psychology Quality of life Institutional review board Clinical research coordinator Clinical research Medicine Research
538	RESEARCH SUBJECTS INFORMATION UPDATED CUMC INSTITUTIONAL REVIEW BOARD (IRB) CONTACT INFORMATION The Columbia University Medical Center (CUMC) Institutional Review Board (IRB) is a committee that independently conducts on Add to Reading List Source URL: www.cumc.columbia.edu Language: English - Date: 2013-10-16 13:31:46 Medical ethics Applied ethics Design of experiments Pharmacology Drug safety Institutional review board Informed consent Human subject research Clinical research coordinator Clinical research Research Ethics
539	Graduate and Research Affairs Division of Research Affairs Add to Reading List Source URL: www.communitychoices.info Language: English - Date: 2014-08-11 13:36:47 Drug safety Research Design of experiments Pharmacology Applied ethics Institutional review board San Diego State University Belmont Report Clinical research coordinator Clinical research Medical ethics Ethics
540	CH Research Ethics Board Non-Interventional Study Consent Form Template Add to Reading List Source URL: www.cdha.nshealth.ca Language: English - Date: 2014-11-29 04:26:17 Applied ethics Medical ethics Science Design of experiments Pharmacology Clinical research coordinator Clinical trial Patient recruitment Informed consent Research Clinical research Pharmaceutical industry

UPDATE