'Human research protection' diaporamas de présentation

Human research protection - PowerPoint PPT Presentation

Human Gene Therapy: Risk Assessment and Regulatory Requirements

Human Gene Therapy: Risk Assessment and Regulatory Requirements

Human Gene Therapy: Risk Assessment and Regulatory Requirements. And Overview of the NIH rDNA Guidelines EMD 545b Lecture #10. NIH Guidelines for Research Involving rDNA Molecules (April, 2002). NIH Guidelines - April 2002. NIH - OBA (Office of Biotechnology Activities)

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751 views • 60 slides
Ethics and Interim Monitoring

Ethics and Interim Monitoring

Ethics and Interim Monitoring. Ethical concerns in general Ethical concerns in trials Monitoring the conduct and findings of trials in progress. Ethical Concerns in all Research. RQ should be important and answerable Benefit should outweigh risk Participants should give consent

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613 views • 49 slides
IRB Responsibilities

IRB Responsibilities

IRB Responsibilities. Marisue Cody, PhD September 6, 2006 Baltimore, MD . Authority & Responsibilities. United States Code (U.S.C.) Code of Federal Regulations (CFR) VHA Directives VHA Handbooks VHA Manuals OHRP Guidance FDA Guidance. Oversight Authority.

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703 views • 45 slides
Understanding Our HRPP and Your Role in the Accreditation Process

Understanding Our HRPP and Your Role in the Accreditation Process

Understanding Our HRPP and Your Role in the Accreditation Process. Introduction. Eugene Oddone, MD, Vice Dean for Research. What is AAHRPP?. Association for the Accreditation of Human Research Protection Programs

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714 views • 41 slides
What Should You Know and Be Doing About Genome Privacy ?

What Should You Know and Be Doing About Genome Privacy ?

What Should You Know and Be Doing About Genome Privacy ?. Ellen Wright Clayton, MD, JD Center for Biomedical Ethics and Society Vanderbilt University. The main point. Making it difficult to link data to an individual is not the only issue Other factors that matter Who controls access?

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298 views • 20 slides
UW-Stout Institutional Review Board (IRB) for the Protection of Human Subjects in Research

UW-Stout Institutional Review Board (IRB) for the Protection of Human Subjects in Research

UW-Stout Institutional Review Board (IRB) for the Protection of Human Subjects in Research. Research Services Updated: 9/01/2013. What is IRB - - And Why Does it Matter to Me??. IRB Institutional Review Board for the Protection of Human Subjects in Research Required by Federal Law

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206 views • 10 slides
Core Responsibilities for Human Research Protection Research Compliance Officers

Core Responsibilities for Human Research Protection Research Compliance Officers

Core Responsibilities for Human Research Protection Research Compliance Officers Robert Brooks, MD, PhD, MBA Associate Director, Research Compliance Education and Policy, ORO 2011 VA Local Accountability for Research Meeting Washington, D.C., June 1-2, 2011. Role of the RCO

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136 views • 3 slides

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