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Clinical research coordinator
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21	Version Date: Version Date: September 2015 © Horizon Health Network - Ethics Services Internal Working Document Page 2 of 10 Horizon Health Network Research Ethics Board Add to Reading List Source URL: en.horizonnb.ca Language: English - Date: 2015-10-08 09:05:45 Medical research Pharmaceutical industry Clinical research Clinical research coordinator Clinical trial Informed consent Confidentiality Good clinical practice Medical privacy
22	Stanford University What Qualifies as Human Subject Research HRPP Policy Guidance Add to Reading List Source URL: researchcompliance.stanford.edu Language: English - Date: 2016-04-12 01:21:49 Clinical research Pharmaceutical industry Design of experiments Medical ethics Research ethics Clinical trial Human subject research Food and Drug Administration Research Institutional review board Clinical research coordinator
23	IRB Compliance With Regulation FERCAP International Conference Dr. Brad Waite Coordinator, International IRB Fellowship Western Institutional Review Board (WIRB) Add to Reading List Source URL: www.fercap-sidcer.org Language: English - Date: 2010-02-19 02:38:03 Medical ethics Clinical research Research ethics Applied ethics Institutional review board Council for International Organizations of Medical Sciences Evaluation Human subject research Food and Drug Administration
24	APPLICATION TO THE MISSOURI UNIVERSITY OF SCIENCE AND TECHNOLOGY CAMPUS INSTITUTIONAL REVIEW BOARD FOR THE PROTECTION OF HUMAN SUBJECTS IN RESEARCH (MSTIRB-1) Add to Reading List Source URL: irb.mst.edu Language: English - Date: 2014-01-22 05:22:59 Medical ethics Clinical research ethics Human subject research Clinical research Design of experiments Institutional review board Informed consent Public Responsibility in Medicine and Research Research Psychology Subject Clinical research coordinator
25	Regulatory Inspection and Quality Improvement of Korean IRBs Young-Mo KOO, AMC, Seoul, KOREA Jeong Mi KIM, KFDA, Seoul, KOREA Trends in the globalization of clinical trials Add to Reading List Source URL: www.fercap-sidcer.org Language: English - Date: 2010-02-19 02:38:05 Clinical research Pharmaceutical industry Clinical trials Design of experiments Food and Drug Administration Clinical research coordinator Good clinical practice
26	Research discoveries can improve people’s health. For more information call: Before you decide to become a research Add to Reading List Source URL: publicfiles.jaeb.org Language: English - Date: 2014-02-10 13:44:14 Clinical research ethics Medical ethics Clinical research Research ethics Office for Human Research Protections Human subject research United States Department of Health and Human Services Research Clinical research coordinator Cooperative Human Tissue Network
27	Microsoft Word - MAGI_Model_CTA v1.07 Abbreviated.doc Add to Reading List Source URL: magiworld.org Language: English - Date: 2015-12-14 16:21:29 Clinical research Pharmaceutical industry Clinical trials Design of experiments Food and Drug Administration Contract research organization Institutional review board Case report form Investigational device exemption Site management organization Clinical research coordinator Monitoring in clinical trials
28	Office of the Vice-President, Research and Innovation Office of Research Ethics Add to Reading List Source URL: www.research.utoronto.ca Language: English - Date: 2016-05-16 14:45:05 Medical ethics Clinical research ethics Human subject research Professional ethics Pharmaceutical industry Research ethics Clinical research coordinator Informed consent Psychology Consent Ethics Debriefing
29	Stanford University HRPP Guidance General Requirements for Informed Consent Add to Reading List Source URL: researchcompliance.stanford.edu Language: English - Date: 2016-04-12 01:21:52 Clinical research Medical ethics Pharmaceutical industry Research ethics Clinical research coordinator Clinical trial Informed consent Human subject research
30	Microsoft Word - SOP - Department of Defense.doc Add to Reading List Source URL: research.missouri.edu Language: English - Date: 2015-07-01 12:42:00 Clinical research ethics Design of experiments Drug safety Institutional review board Regulatory compliance Common Rule IRB Clinical research coordinator

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