<--- Back to Details
First PageDocument Content
Clinical research ethics / Medical research / Ethics / Research / Design of experiments / Drug safety / Institutional review board / Regulatory compliance / Public Responsibility in Medicine and Research / Office for Human Research Protections / IRB / Clinical research coordinator
Date: 2015-07-01 12:45:56
Clinical research ethics
Medical research
Ethics
Research
Design of experiments
Drug safety
Institutional review board
Regulatory compliance
Public Responsibility in Medicine and Research
Office for Human Research Protections
IRB
Clinical research coordinator

Microsoft Word - SOP - IRB Membership.docx

Add to Reading List

Source URL: research.missouri.edu

Download Document from Source Website

File Size: 29,31 KB

Share Document on Facebook

Similar Documents

Institutional Review Board Wake Forest University – Reynolda Campus Certificate of Confidentiality Checklist Note: A Certificate of Confidentiality will not be issued to an applicant co

DocID: 1uZkR - View Document

Institutional Review Board . ... . .

DocID: 1ubXP - View Document

University of Pennsylvania  Institutional Review Board O Is IRB Review Required? The first question one should consider when assessing the requirement for IRB review is whether the activity meets the regulatory defini

DocID: 1tsSK - View Document

Reliance Memorandum of Understanding Between and Among the University of California Campuses, UC Division of Agriculture and Natural Resources, and Lawrence Berkeley National Laboratory for Institutional Review Board Rev

DocID: 1to8J - View Document

INSTITUTIONAL REVIEW BOARD HUMAN SUBJECTS RESEARCH DETERMINATION FORM Instructions: Complete this form to help determine if your project qualifies as research that involves the use of human participants. You are not r

DocID: 1tdGE - View Document