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Office for Human Research Protections
Results: 393

#	Item
21	Stanford University HRPP International Research Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-04-12 01:21:49 Clinical research ethics Medical ethics Clinical research Design of experiments Human subject research Institutional review board Public Responsibility in Medicine and Research Office for Human Research Protections Certified IRB Professional Clinical research coordinator
22	Title: FO 306 – Institutional Review Board Authorization Agreements for Review by External IRBs (IRB Reliance) Department: Sparrow Institutional Review Board 1.0 Policy: Add to Reading List Source URL: www.sparrow.org Language: English Clinical research ethics Medical ethics Design of experiments Clinical research Institutional review board Office for Human Research Protections Common Rule Grant IRB Human subject research Cooperative Human Tissue Network Clinical research coordinator
23	Consent Waiver) Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-04-12 01:21:49 Clinical research ethics Medical ethics Human subject research Clinical research Research ethics Office for Human Research Protections Informed consent Food and Drug Administration Institutional review board Clinical research coordinator
24	The IRB staff and the IRBs have the following written policies and procedures for determining the risks to vulnerable populations as defined in applicable federal regulations, and specifically for determining the require Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-04-12 01:21:50 Clinical research ethics Research Contact Office for Human Research Protections Applied ethics
25	October 26, 2011 Jerry Menikoff, MD, JD Office for Human Research Protections Department of Health and Human Services 1101 Wootton Parkway, Suite 200 Rockville, MD 20852 Add to Reading List Source URL: www.faseb.org Language: English - Date: 2011-10-27 09:07:10
26	SOP 24 - OHSRP REPORTING TO THE OFFICE FOR HUMAN RESEARCH PROTECTIONS (OHSRP) AND THE FOOD AND DRUG ADMINISTRATION (FDA) REGARDING UNANTICIPATED PROBLEMS, SERIOUS OR CONTINUING NONCOMPLIANCE, OR TERMINATIONS OR SUSPENSIO Add to Reading List Source URL: ohsr.od.nih.gov Language: English - Date: 2015-09-29 17:00:19
27	See Does My Project Need IRB Review? If there is any question whether your project is human subject research you must submit this form to the IRB. Complete all sections then email to . Th Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-01-27 16:54:35 Clinical research Pharmaceutical industry Medical ethics Design of experiments Human subject research Clinical trial Office for Human Research Protections Food and Drug Administration Public Responsibility in Medicine and Research Clinical research coordinator
28	DOCUMENTATION OF TRAINING IN HUMAN SUBJECT PROTECTION (FOR INVESTIGATORS AND DIRECTORS) Institutional Review Board The Federal Office for Human Research Protections (OHRP) requires Principle Investigators of Add to Reading List Source URL: www.virginiawestern.edu Language: English - Date: 2015-04-01 12:10:55
29	DOCUMENTATION OF EDUCATION ON THE PROTECTION OF HUMAN SUBJECTS For IRB Members Only The Federal Office for Human Research Protections (OHRP) requires IRB members to Add to Reading List Source URL: www.virginiawestern.edu Language: English - Date: 2015-04-01 12:10:40
30	Microsoft Word - 02 Alex Capron _US law and governance__edit_.doc Add to Reading List Source URL: www.sal.org.sg Language: English - Date: 2014-05-06 04:22:39 Ethics Medical ethics Research ethics Medical research Pharmacology Office for Human Research Protections Institutional review board Declaration of Helsinki Belmont Report Clinical research Research Medicine