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Clinical research coordinator
Results: 1108

#	Item
971	Note-To-File: Explanation of Irregularity / Non-Compliance IRB Number: Add to Reading List Source URL: www.visn2.va.gov Language: English - Date: 2013-01-31 13:35:47 Adverse event Clinical research coordinator Clinical research Pharmaceutical industry Research
972	INSTITUTIONAL REVIEW BOARD (IRB) SUBMISSION REQUIREMENTS A. Protocol Preparation. Protocols will be formulated within the mission areas of Coast Guard (CG) or the Department of Homeland Security (DHS). The problem or obj Add to Reading List Source URL: www.uscg.mil Language: English Pharmaceutical sciences Science Food and Drug Administration Pharmacology Drug safety Clinical research coordinator Institutional review board Clinical trial Investigational New Drug Clinical research Research Pharmaceutical industry
973	SAMPLE EXEMPTION REQUEST ABSTRACT Summary of the proposed research including purpose of study and proposed methodology. BRIEF RATIONALE OF OBJECTIVES Provide an introduction section that outlines the rationale for the st Add to Reading List Source URL: www.uscg.mil Language: English Autonomy Informed consent Consent Risk Clinical research coordinator Institutional review board Ethics Medical ethics Clinical research
974	Report of Serious and Unexpected Adverse Event FORM For any section in which additional space is needed, complete on plain bond paper. Report Type: ____Initial ___ Follow-up ___ Medical Monitor IRB Log No: A- Add to Reading List Source URL: www.uscg.mil Language: English Pharmaceutics Pharmacology Adverse event Pharmaceutical sciences Clinical trial Clinical research coordinator Clinical research Pharmaceutical industry Research
975	1 Informed Consent Checklist –Basic and Additional Elements 45 CFR § [removed]A statement that the study involves research An explanation of the purposes of the research Add to Reading List Source URL: www.nd.gov Language: English - Date: 2008-02-22 15:17:25 Human subject research Scientific method Clinical research coordinator Clinical research Research Ethics
976	RESEARCH USE Statutes, Rules and Regulations Pertaining to Vital Records Data Missouri state statutes[removed], [removed], &[removed]and the Code of State Regulations (19 CSR[removed]Access to Vital Records) allow for th Add to Reading List Source URL: health.mo.gov Language: English - Date: 2014-12-30 12:00:03 Research Drug safety Medicine Science Institutional review board Department of Health Clinical research coordinator Clinical research Design of experiments Pharmacology
977	Fort Peck Institutional Review Board Request for Designation of Research as Exempt from the Requirement of Institutional Review Board Review[removed]) Add to Reading List Source URL: www.fpcc.edu Language: English - Date: 2013-02-01 16:14:16 Science Institutional review board Human subject research Psychology Grant Health Insurance Portability and Accountability Act Clinical research coordinator Cooperative Human Tissue Network Clinical research Ethics Research
978	REPORT OF SERIOUS AND UNEXPECTED ADVERSE EVENT FORM For any section in which additional space is needed, complete on plain bond paper. Report Type: ____Initial ___ Follow-up ___ Medical Monitor IRB Log No: AStudy Title: Add to Reading List Source URL: www.uscg.mil Language: English Pharmacology Pharmaceutical sciences Pharmaceutics Adverse event Clinical trial Clinical research coordinator Clinical research Pharmaceutical industry Research
979	Re-review of previously approved research Add to Reading List Source URL: www.health.state.mn.us Language: English - Date: 2012-03-09 16:04:00 Drug safety Research Scientific method Institutional review board Science Clinical research coordinator Clinical research Design of experiments Pharmacology
980	Step-by-Step Instructions for Registering an Institutional Review Board (IRB) Version Date[removed]This form is used by institutions or organizations operating IRBs that review: 1. Research involving human subjects co Add to Reading List Source URL: www.hhs.gov Language: English - Date: 2014-08-21 00:36:35 Design of experiments Drug safety Scientific method Science Institutional review board Office for Human Research Protections Public Responsibility in Medicine and Research Clinical research coordinator Clinical research Research Pharmacology

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