Basic Documents (Must Submit)

Basic Documents (Must Submit)

Review Checklist. Basic Documents (must submit). Review Checklist UPMREB FORM 2(A)2012. Printed Registration and Application Form UPMREB FORM 2(B)2012. Study Protocol Assessment Form UPMREB FORM 2(C)2012. RGAO Endorsement. Study Protocol. Data collection forms (including CRFs).

Appendix B: Business Ethics in Medical Research Panelists

Appendix B: Business Ethics in Medical Research Panelists

Appendix B: Business Ethics in Medical Research Panelists. Salvador Cruz-Flores, MD. Dr. Cruz received his medical degree from the Universidad Autonoma de Nuevo Leon in Monterrey Mexico, where he also completed residencies in internal medicine and neurology.

Vulnerable Populations Checklists- Cognitively Impaired

Vulnerable Populations Checklists- Cognitively Impaired

Vulnerable Populations Checklists- Cognitively Impaired. IRB-HSR or UVA Study Tracking. A person may be cognitively impaired due to any of the following. A psychiatric disorder (e.g., psychosis, neurosis, personality or behavior disorders). An organic impairment (e.g., dementia, Alzheimer s).

The Emergency Use of An

The Emergency Use of An

AlexianBrothersHospital Network. Institutional Review Board. ADVERSE EVENT REPORTING INSTRUCTIONS. For Drug/Biological Studies. Any adverse drug/biological experience that is serious, unexpected, and related or possibly related to the investigational.

FREC - Ethics Amendments Application Form (Nov 2016)

FREC - Ethics Amendments Application Form (Nov 2016)

De Montfort University. Faculty of Health & Life Sciences. Faculty Research Ethics Committee. AMENDMENT/EXTENTION APPLICATION FORM. PLEASE READ SUBMISSION GUIDELINES BEFORE COMPLETING THIS FORM. Further information and application forms are available at.

Experimental Medicine Cell Bank Service

Experimental Medicine Cell Bank Service

SUPPLEMENTARY INFORMATION. Experimental Medicine Cell Bank Service. Rationale: Ensuring Bio-integrity. The division of Experimental Medicine has an excellent research profile that spans from basic science to translational medicine, from bench to bedside.

Alexian Brothers Hospital Network

Alexian Brothers Hospital Network

Application to Continue (Renew) a Previously Approved IRB STUDY/HDE. At AMITA HEALTH. AMITA Health (ABHN or AMH)IRB. Project Title(optional). Principal Investigator. Please provide allrequested information/documents pertaining to the above referenced.

Appendix a If Placebo Is Being Used

Appendix a If Placebo Is Being Used

UT SYSTEM IRB RECIPROCITY AGREEMENT. APPLICATION FOR ADDITION OF SITE. Information for Overall Principal Investigator In addition to submitting an application to your organization s IRB (designated as Reviewing IRB ), an application for addition of site.

TITLE:Islington Pharmacy Based Cardiovascular Risk Assessment Pilot

TITLE:Islington Pharmacy Based Cardiovascular Risk Assessment Pilot

TITLE:Islington Pharmacy Based Cardiovascular Risk Assessment Pilot. AUTHOR:Pharmacy Pilot Steering Group. MEETING:Briefing Paper for the Pharmacy Contract Meeting June 10th. 1. Background / rationale. 2. Pilot overview. 3. Patient pathway. 4. Recruitmentof pilot sites. 5. Pilot Training.

Application for IRB Review

Application for IRB Review

Application for IRB Review. Projects which involve procedures that pose greater than minimal risk, or in which the principal purpose is to study vulnerable subjects, require additional provisions to ensure that the ethical principles of beneficence.

Essential Documents Binder

Essential Documents Binder

UF Regulatory Binder Template. Section 1: IRB Correspondence. This section should contain your IRB correspondence and approvals for the study. To be sure your file is complete, you may want to check it against the IRB file to assure completeness. IRB Submission Tracking Log.

Research Project Description for Use with HREA

Research Project Description for Use with HREA

Research Project Description for use with HREA. Title and Resources. Background to the Project. Project Design. Approved name. Trade name (if any). Supplier of drug/device (e.g. manufacturer/pharmacy). Approved therapeutic indication, dosage/duration in Australia. Believed mode of action.

Biobank Literature Update Week 43 (2015)

Biobank Literature Update Week 43 (2015)

Biobank literature update week 43 (2015). 1 The Genotype-Tissue Expression (GTEx) Project. Carithers LJ, Moore HM.Biopreserv Biobank2015; 13:307-308. 2 Times Are Changing: 35 Years of Human Biospecimen Procurements for the National Disease Research.

Mrc Uk the Gambia

Mrc Uk the Gambia

MRC UNIT, THE GAMBIA. JOB DESCRIPTION. HEAD OF COMMUNICATIONS. 1.Job title:Head of Communications. Established in 1947, the Medical Research Council in The Gambia has an international reputation for ground-breaking research into some of the leading causes.

Elizabeth City State University

Elizabeth City State University

Institutional Review Board for the protection of human participants in research. Request for Certification of Exempt Status. Instructions: Submit completed form, with signatures, and any applicable attachments, to the IRB Office. Section I: General Information.

University of Texas Southwestern

University of Texas Southwestern

UNIVERSITY OF TEXAS SOUTHWESTERN. Brain Tissue/Body Fluid Request. Complete this form and submit to. Roger N. Rosenberg, M.D., Director - ADC. Department of Neurology and Neurotherapeutics. University of Texas Southwestern MedicalCenter. 5323 Harry Hines Boulevard, MC: 9036.