Medical Research
Request for IRB Advisory Review of Ethics Plan
Request for IRB Advisory Review of Ethics Plan. This form is to be submitted by a St. Olaf faculty or staff member to . Please check and attach all that apply. Ethics Plan for Inquiries Involving People(required).
Institutional Certification for Single Site Studies
Institutional Certification for Single Site Studies. Click here to enter a date. GDS Program Administrator. Institute: , NIH, DHHS. Re: Institutional Certification of East Carolina University to accompany submission of the dataset for the study entitled to an NIH-designated data repository.
University of Texas at Arlington Institutional Animal Care and Use Committee Scoring Endpoints
University of Texas at Arlington Institutional Animal Care and Use Committee Scoring Endpoints in Tumor Studies in Rats and Mice. A.BACKGROUND INFORMATION. a.Tumor (cancer)researchin animals is an importantexperimental activitywhichalsorequiresconsideration of theeffect of thetumoron the animal.
D1. Informed Consent and Informed Choice
A Cross-Cultural Introduction to Bioethics. D1. Informed Consent and Informed Choice. Chapter Objectives. The relationships between health professionals and patients are changing in all societies to give more voice to patients. The same is true in other.
Initial Device Study Application
Initial Device Study Application. Single Site Study. As the Principal Investigator, I agree to uphold ethical standards and practices in research and conduct this research in accordance with applicable federal regulations, state and local laws, and requirements of Aspire IRB as follows.
Code Number (For Official Use Only)
HEALTH ETHICS COMMITTEE. Application form for clinical trials other than. of medicinal products. Code number (for official use only). Research identification. Tick as appropriate. Clinical research. Experimental research. Research involving investigational medical devices.
Aging Clinical Research Center
StanfordCenter for Narcolepsy Research. Donor Program. Information about the Donor Program. The StanfordCenter for Narcolepsy Research is primarily funded by the National Institute of Health. The Center for Narcolepsy was established in the early 1980s.
University of North Dakota Human Subjects Review Form
IRB Application for Research Protocols. Please provide the information requested below. SUMMARY OF THE PROTOCOL. Include a brief statement for each of the following. Borgess IRB approved for use: V5 8/2014. Bronson IRB Reviewed & Approved: V5 8/2014. Research Team Members.
The Social Science Stem Cell Initiative: Capacitybuilding and Awareness Raising
ESRC Investment in. The Social Science Stem Cell Initiative: CapacityBuilding and Awareness Raising. Call Specification May 2006. Executive Summary. As part of its investment in the social and economic aspects of Stem Cell science the Economic and Social.
PRESS RELEASE European Association of Urology (EAU) 28Th Annual EAU Congress
PRESS RELEASE European Association of Urology (EAU) 28th Annual EAU Congress. For immediate release. New study evaluates incidence and mortality of prostate cancer after termination of PSA-based screening.
Guidelines for Emerging Interdisciplinary Research
Guidelines for Emerging Interdisciplinary Research. Under the UP Charter of 2008, UP is envisioned to significantly strengthen its research culture and increase nationally and globally relevant research output. The OVPAA supports research in the university under the following general guidelines.
Research Review Application
Research/Project Review Application. This form fulfills both Research and IRB requirements for HealthEast. Please complete all questions, even if you are not applying for IRB approval. a.Principal Investigator(s): Mailing Address: Telephone: FAX: Email.
SOP Funding Review
This document describes the HSD/IRB procedure for the assessment of anexternal grant application. The purpose of the assessment is to. 1.1Comply with the federal requirement for IRB review of federal grants (45 CFR 46.103(f)).
Protocol-Specific Guidelines Formanagement of Investigational Product(S)
Please use this template as applicable 1) to establish dispensing procedures with a research team and 2) to train backup pharmacy staff. Please refer to a study protocol and other relevant documents for study-specific information. If information is not.
Original Author: Christopher Moskaluk
LCBRN Standard Operating Procedure. SOP#: 12Version#:1Effective Date: 09/01/2011. SOP Title:Obtaining Informed Consent. Original author: Sandra Burks. Author of latest version: Sandra Burks. Authorizer: Christopher Moskaluk, LCBRN Principal Investigator. Last review date:08/15/2011.
Application for Review of Human Subjects Research
Application for Review of Human Subjects Research.
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