'Informed consent process' diaporamas de présentation

Orientation for New Clinical Research PERSONNEL Module 1

Orientation for New Clinical Research PERSONNEL Module 1. Presented by NC TraCS Institute UNC Office of Clinical Trials UNC Network of Clinical Research Professionals. Overview of orientation program & Introduction to clinical research. Marie Rape, TraCS Regulatory Core .

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Human Gene Therapy Application Procedures

Human Gene Therapy Application Procedures. Robert J. Hashimoto The University of Louisville April 5, 2001. INTRODUCTION.

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Good Clinical Practices

Good Clinical Practices. Presented By :. Good clinical Practices.

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IRB Review: Beyond the Basics

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Human Subject Issues in Research: Informed Consent

Human Subject Issues in Research: Informed Consent . Jill M. Baren, MD. What is Ethics?. The study of standards and conducts and moral judgment The system or code of morals of a particular person, religion, group, or profession. Identifying Ethical Issues.

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Supervisor/supervisee ethical expectations: What goes on behind closed doors?

Supervisor/supervisee ethical expectations: What goes on behind closed doors?. Jeffrey E. Barnett, Psy.D., ABPP Karen Strohm Kitchener, Ph.D. Jenny Cornish, Ph.D., ABPP Rodney Goodyear, Ph.D. Overview. Introduction (Jeff Barnett) Methods/Results (Jenny Cornish)

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Preparing For A VA Compliance Audit

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ICH-GCP & FDA Regulations Differences

ICH-GCP & FDA Regulations Differences. John D. Burke Director, Human Subjects Protection Program University Of Louisville April 21, 2009. International Conference on Harmonisation (ICH).

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Objective 1.3: Discuss how and why particular research methods are used at the cognitive level of analysis.

Objective 1.3: Discuss how and why particular research methods are used at the cognitive level of analysis. Research at the cognitive level.

877 views • 29 slides

Doctor of Audiology Program Director Survey 2013

Doctor of Audiology Program Director Survey 2013. Diana C. Emanuel, Ph.D. Towson University. Praxis. Summary: Program directors were not informed and did not provide input on praxis changes but changes have impacted their programs. CSDCAS. Summary:

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NATIONAL ATAXIA REGISTRY

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IMPAACT 2010 Protocol Specifications for Recruitment, Screening, and Enrollment

IMPAACT 2010 Protocol Specifications for Recruitment, Screening, and Enrollment. Protocol References. Recruitment Context.

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Payment Models for Shared Decision Making: Systematic Review and Recommendations

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Ethical considerations of HIV research in Thailand: the HIV-NAT as a case study

Ethical considerations of HIV research in Thailand: the HIV-NAT as a case study Praphan Phanuphak, M.D., Ph.D. Faculty of Medicine, Chulalongkorn University & The Thai Red Cross AIDS Research Centre Bangkok, Thailand HIV-NAT The HIV N etherlands A ustralia T hailand Research Collaboration

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Elements of Ethical Review of Study Documents

Elements of Ethical Review of Study Documents. Dr.C.H.Shashindran Director-Professor & Head Department of Pharmacology JIPMER. Review. All properly submitted applications should be reviewed in a timely fashion and according to an established review procedure.

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Objective 4: Explain informed decision-making and the informed consent process

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