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Understanding Research: Getting Your Project Ready for the IRB Jill Stoltzfus, Ph.D. Director, Research Institute stoltzj@slhn.org.
Documents Understanding Research: Getting Your Project Ready for the IRB Jill Stoltzfus, Ph.D. Director,...

Slide 1Understanding Research: Getting Your Project Ready for the IRB Jill Stoltzfus, Ph.D. Director, Research Institute [email protected] Slide 2 Todays Objectives Present…

Institutional Conflict of Interest and Commercialization Joyce Brinton Director, Office for Technology and Trademark Licensing Harvard University Intellectual.
Documents Institutional Conflict of Interest and Commercialization Joyce Brinton Director, Office for...

Slide 1 Institutional Conflict of Interest and Commercialization Joyce Brinton Director, Office for Technology and Trademark Licensing Harvard University Intellectual Property…

Presented by The Research Integrity Office. Knowledgeable ▪ The regulations, research, the IRB process Thorough Thoughtful Collaborative ▪ With.
Documents Presented by The Research Integrity Office. Knowledgeable ▪ The regulations, research, the IRB...

Slide 1 Presented by The Research Integrity Office Slide 2  Knowledgeable ▪ The regulations, research, the IRB process  Thorough  Thoughtful  Collaborative…

IRB 101: IRB Review Criteria; Tips for Submission Columbia University Medical Center IRB July 14, 2005.
Documents IRB 101: IRB Review Criteria; Tips for Submission Columbia University Medical Center IRB July 14,...

Slide 1 IRB 101: IRB Review Criteria; Tips for Submission Columbia University Medical Center IRB July 14, 2005 Slide 2 Objectives 1.Describe how submissions are routed for…

Quick Facts about Exempt Research No continuing review required IRB Reviewer makes Exempt determination 6 OHRP & 4 FDA categories(1 category overlaps)
Documents Quick Facts about Exempt Research No continuing review required IRB Reviewer makes Exempt...

Slide 1 Slide 2 Quick Facts about Exempt Research No continuing review required IRB Reviewer makes Exempt determination 6 OHRP & 4 FDA categories(1 category overlaps)…

Taking the Plunge: Facilitating and Monitoring Collaborative Research and IRB Authorization Agreements Charles Hite Director, Biomedical & Research Ethics.
Documents Taking the Plunge: Facilitating and Monitoring Collaborative Research and IRB Authorization...

Slide 1 Taking the Plunge: Facilitating and Monitoring Collaborative Research and IRB Authorization Agreements Charles Hite Director, Biomedical & Research Ethics Slide…

Human Participants Research at the University of Northern Iowa
Documents Human Participants Research at the University of Northern Iowa

Human Participants Research at the University of Northern Iowa Information for Students, Faculty & Staff at UNI Objectives Understand the historical context in which…

GEARING UP FOR AAHRPP A Presentation for IRB Members – March 2011 Beverley Esparza, CIP Assistant Director, Human Research Protections.
Documents GEARING UP FOR AAHRPP A Presentation for IRB Members – March 2011 Beverley Esparza, CIP Assistant....

GEARING UP FOR AAHRPP A Presentation for IRB Members â March 2011 Beverley Esparza, CIP Assistant Director, Human Research Protections * Learning Objectives â March 2011…

1 IRB Basics and Tips for Navigating the IRB Review Process.
Documents 1 IRB Basics and Tips for Navigating the IRB Review Process.

* IRB Basics and Tips for Navigating the IRB Review Process * What is the âCommon Ruleâ? Ethical Principles A Brief History Navigating the Review Process Three forms of…

TUN IRB: The Basics February 26, 2015. IRB Function Review human-subject research Ensure the rights & welfare of human subjects are adequately protected.
Documents TUN IRB: The Basics February 26, 2015. IRB Function Review human-subject research Ensure the rights....

TUN IRB: The Basics TUN IRB: The Basics February 26, 2015 IRB Function Review human-subject research Ensure the rights & welfare of human subjects are adequately protected…

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