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Clinical research coordinator
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181	SG-EN-TRA-00 (SV) Add to Reading List Source URL: www.finlex.fi Language: English Science Institutional review board Clinical trial Ethics Committee Informed consent Human subject research Dignity Clinical Trials Directive Clinical research coordinator Clinical research Research Ethics
182	Submission on the consultation paper on the Development of a table of standard costs for conducting Clinical Trials in Australia Add to Reading List Source URL: www.ihpa.gov.au Language: English - Date: 2014-04-09 08:00:00 Clinical trials Science Design of experiments Pharmacology Clinical research coordinator Costs Clinical research Pharmaceutical industry Research
183	Submission on the consultation paper on the Development of a table of standard costs for conducting Clinical Trials in Australia Add to Reading List Source URL: www.ihpa.gov.au Language: English - Date: 2013-06-19 19:30:20 Research Medicine Clinical trial Clinical research coordinator Allied health professions Health care Clinical research Pharmaceutical industry Health
184	MDH_IRB FORM 3(E)2012: EARLY STUDY TERMINATION APPLICATION FORMEarly Study Termination Application Form INSTRUCTIONS TO THE PRINCIPAL INVESTIGATOR: This form is required to apply for premature termination or Add to Reading List Source URL: www.maniladoctors.com.ph Language: English Pharmaceutical industry Technology Science Pharmacology Clinical research coordinator Clinical research Email Research
185	Research Site Submission Form Add to Reading List Source URL: research.unc.edu Language: English - Date: 2014-01-13 15:25:24 Science Medical ethics Pharmaceutical industry Design of experiments Pharmacology Clinical research coordinator Clinical trial Institutional review board Investigational New Drug Clinical research Research Ethics
186	Standard Operating Procedures for Queensland Health Research Governance Officers Add to Reading List Source URL: health.qld.gov.au Language: English - Date: 2013-11-28 01:02:30 Research Medicine Design of experiments Pharmacology Nursing research Institutional review board Clinical trial Clinical research coordinator Clinical audit Clinical research Health Pharmaceutical industry
187	Responsibilities of Staff in Human Subjects Research The University of North Carolina at Chapel Hill Add to Reading List Source URL: research.unc.edu Language: English - Date: 2013-03-14 13:58:16 Applied ethics Research Design of experiments Pharmacology Drug safety Institutional review board Informed consent Human subject research Clinical research coordinator Clinical research Ethics Medical ethics
188	SESLHD PROCEDURE COVER SHEET NAME OF DOCUMENT Clinical Forms – Creation and Revision Add to Reading List Source URL: www.seslhd.health.nsw.gov.au Language: English - Date: 2014-03-07 00:05:19 Healthcare management Medical record Document management system Clinical governance Nursing in the United Kingdom Clinical research coordinator Health informatics tools National Health Service Health Medicine
189	Initial Review Submission Form Add to Reading List Source URL: research.unc.edu Language: English - Date: 2014-01-13 15:30:10 Health Institutional review board Clinical research coordinator Investigational New Drug Clinical trial Site management organization WIRB National Institutes of Health Human subject research Research Clinical research Medicine
190	Submission on the consultation paper on the Development of a table of standard costs for conducting Clinical Trials in Australia Add to Reading List Source URL: www.ihpa.gov.au Language: English - Date: 2013-06-19 19:30:21 Pharmacology Research Pharmaceutics Drug discovery Design of experiments Clinical trial GlaxoSmithKline Drug development Clinical research coordinator Pharmaceutical industry Pharmaceutical sciences Clinical research

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