Principal Investigator/Program Director (Last, first, middle).PHS 398/2590 Other Support.Kenneth Kopecky, Ph.D.Vanderbilt University Medical Center (John D Boice, Jr, PI) 04/01/10 03/31/15 0.96 cal mo.Cancer Mortality among Military Participants at US Nuclear Weapons Tests
Stanford University Required Questions for the Protocol Application.Research Compliance Office Medical.1. Describe steps taken to minimize the possibility of coercion or undue influence.2. Provide an assessment of the importance of the knowledge expected to result from this study
The role and responsibilities of the non-local IRB;.An agreement that the entities will comply with relevant federal regulations;.A written agreement between the performance site where the research is to be conducted and the non-local IRB or its institution;
Insert checked box when formatting for IRB review for the site where research will occur.MOUNT SINAI BETH ISRAEL MOUNT SINAI ST. LUKE S.MOUNT SINAI ROOSEVELT.CONSENT FORM TO VOLUNTEER IN A RESEARCH STUDY.IRB (HS#) #: Form Version Date
Checklist of Items to be Submitted to the IRB for Continuing Review.All documents must be submitted as a hardcopy to the IRB Office (15 Kneeland Street, Tupper 1) or by interoffice mail to Box #817. This checklist is for your use and does not need to be submitted to the IRB
University Hospitals Bristol Research and Development Department.Glossary of terms.ABPI: Association of the British Pharmaceutical Industry. A trade association for UK pharmaceutical companies
BIOMEDICAL ADVERSE EVENT REPORT.UCSD Human Research Protections Program.REPORT OF UNANTICIPATED PROBLEM INVOLVING RISK TO SUBJECT OR OTHERS.Section 1: IDENTIFYING INFORMATION.*If study does not use a study unique identifier, enter subject s initials
MRC UNIT THE GAMBIA.Job Description.Project Support Manager (Research Training and Career Development).1. Job title: Project Support Manager (Research Training).Established in 1947, the Medical Research Council The Gambia has an international reputation
IRB Committee C Consent Form Template IRB File # ______.Revised 120613 Page 1 of 11.CONSENT FORM AND INFORMATION.Title of Study.STUDY TO BE CONDUCTED BY.Principal Investigator.Study Sponsor
Profile: DCEMRI Quantification.QIBA DCEMRI Sub-committee.Draft Version 0.4.I. CLINICAL CONTEXT Jeff E.Few sentences about DCEMRI QIBA committee.High level parapgrah about DCEMRI and the clinical context.Response to therapy
D. Continuing Review
Allina Health IRB Submissions.What must be submitted to Quorum Review IRB?.How do I submit studies to Quorum Review IRB?.Initial Submissions.Step 1: Access the appropriate Quorum Review IRB submission forms
IRB-02 PRIMARY REVIEWER CHECKLIST.CONTINUING REVIEW.Protocol & Primary Reviewer Identification.Principal Investigator.Study Expiration Date.Primary Reviewer.If your answer to question #1 OR #2 is Yes, STOP HERE. Call the Human Subjects Office at 335-6564
THE ROYAL VICTORIAN EYE AND EAR HOSPITAL.HUMAN RESEARCH & ETHICS COMMITTEE.Annual Progress Report.Approval of research projects by the RVEEH HREC is conditional upon the provision of an annual report within 12 months of approval. Please provide an electronic copy to the HREC Secretary
Title of research.Research Capacity in Health Librarianship: The ReCAP Project.To identify key priorities and barriers for research development in health librarianship.To gain consensus on key questions to be included in a national survey for research development in health librarianship
Last data updates: 06 January 2016.Li, L.L., Ding, G.H., Feng, N., Wang, M.H. and Ho, Y.S.* (2009), Global stem cell research trend: Bibliometric analysis as a tool for mapping of trends from 1991 to 2006. Scientometrics, 80 (1), 39-58