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2024

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To pay or not to pay: Is that the question?

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OHSRP Education Series

January 11, 2024/Christine Grady

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2023

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The Single IRB Model at the NIH: Principles, Processes, and Pitfalls

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OHSRP Education Series

November 2, 2023/Jeffrey Rollins and Shirley Rojas

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Considerations for Informed Consent in Gene Therapy Trials

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OHSRP Education Series

October 5, 2023/Daniel Kavanagh, PhD, RAC

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Emergency Preparedness for Investigators

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OHSRP Education Series

September 7, 2023/Heather Bridge, Aaron Salter, Paula Barton-Mann, Arman Sabet-Kashani & Astrid Smith

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More Ethics or More Compliance: What was Dr. Beecher Trying to Tell us?

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OHSRP Education Series

August 3, 2023/Quincy J. Byrdsong, Ed.D.

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Regulations and the Secrets of Big Data: Public, Private, or What?

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OHSRP Education Series

June 1, 2023/Ivor Pritchard, Ph.D.

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Tips & Tricks for Avoiding Stips: How to Increase the Odds of Achieving Speedy IRB Approval

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Protocol Navigator Work Group Meeting

May 11, 2023/Julie Eiserman

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Ethics of Sharing Individual-level Data from Research with Human Subjects

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OHSRP Education Series

May 4, 2023/Saskia Hendriks, MD, PhD

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A How to Guide: The Use of Social Media in Research

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OHSRP Education Series

April 13, 2023/Brenda Curtis, PhD, MsPH

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Preventing Unplanned Pregnancies in Clinical Research--Balancing Science, Safety, and Ethics

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OHSRP Education Series

March 2, 2023/ Evan Myers, MD, MPH, Walter L. Thomas Distinguished Professor of Obstetrics and Gynecology at Duke University School of Medicine

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Implementing the NIH Data Management and Sharing Policy within the NIH IRP

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OHSRP Education Series

February 16, 2023/Taunton Paine and Chuck Dearolf

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The What, When and Why of Investigator Financial Conflict of Interest Review

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OHSRP Education Series

January 19, 2023/Tonia Smith Awoniyi, Heather Bridge and Jonathan Green

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Considerations for Modernizing the Informed Consent Process

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OHSRP Education Series

December 1, 2022/Nichelle Cobb and Christine Suver

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PROTECT Electronic IRB (eIRB) Go-Live Town Hall

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OHSRP Education Series

November 17, 2022/Jonathan Green, Nicole Grant and Tiffany Gommel

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FDA Investigational Device Exemptions (IDE): Overview and Application to Research Involving MRI

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OHSRP Education Series

October 6, 2022/William Pritchard, Alan Koretsky and Lauren Reoma

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NIH IRB Expectations for Return of Secondary Genomic Findings to Research Participants

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OHSRP Education Series

September 1, 2022/Sara Chandros Hull and Benjamin E. Berkman

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Re-consent and Subject Notification: Expectations and Flexibilities for Complying with the Common Rule

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OHSRP Education Series

August 4, 2022/Julie Eiserman and Tiffany Gommel

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Overview: NIH Multi-Site Protocol Processes

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Protocol Navigator Meeting

July 14, 2022/Jeffrey Rollins and Shirley Rojas

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(If login is required, use NIH username followed by nih.gov. For example, if John Doe’s NIH user name is doej, enter the following to logon: doej@nih.gov)

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Electronic IRB (eIRB) System Demo and Change Considerations

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OHSRP Education Series

June 2, 2022/Sue Tindall and Meredith Mullan

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The Informed Consent Process-The Good, the Bad & the Ugly

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OHSRP Education Series

May 5, 2022/Katherine W. Todman and Carol Squires

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Investigational Devices: What you need to know and Sponsor and Investigator Responsibilities

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OHSRP Education Series

April 7, 2022/Jonathan Green and Lisa Goldfeder

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Determining Whether Your Project Might Require an Exemption or IRB Review

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NCI CCR Clinical Research Forum

March 21, 2022/Julie M. Eiserman

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Health Literacy Considerations for Clinical Trial Communication and Decision Making

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OHSRP Education Series

March 3, 2022/Dr. Aisha Langford

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Regulatory Considerations in Natural History Studies

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OHSRP Education Series

February 03, 2022 / Jonathan Green

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OHSRP Town Hall

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OHSRP Education Series

January 13, 2022 / Jonathan Green, Tiffany Gommel, Heather Bridge and Meredith Mullan

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Versions Compared

Old Version 173

New Version 174

Key

2024

To pay or not to pay: Is that the question?

OHSRP Education Series

2023

The Single IRB Model at the NIH: Principles, Processes, and Pitfalls

OHSRP Education Series

Considerations for Informed Consent in Gene Therapy Trials

OHSRP Education Series

Emergency Preparedness for Investigators

OHSRP Education Series

More Ethics or More Compliance: What was Dr. Beecher Trying to Tell us?

OHSRP Education Series

Regulations and the Secrets of Big Data: Public, Private, or What?

OHSRP Education Series

Tips & Tricks for Avoiding Stips: How to Increase the Odds of Achieving Speedy IRB Approval

Protocol Navigator Work Group Meeting

Ethics of Sharing Individual-level Data from Research with Human Subjects

OHSRP Education Series

A How to Guide: The Use of Social Media in Research

OHSRP Education Series

Preventing Unplanned Pregnancies in Clinical Research--Balancing Science, Safety, and Ethics

OHSRP Education Series

Implementing the NIH Data Management and Sharing Policy within the NIH IRP

OHSRP Education Series

The What, When and Why of Investigator Financial Conflict of Interest Review

OHSRP Education Series

Considerations for Modernizing the Informed Consent Process

OHSRP Education Series

PROTECT Electronic IRB (eIRB) Go-Live Town Hall

OHSRP Education Series

FDA Investigational Device Exemptions (IDE): Overview and Application to Research Involving MRI

OHSRP Education Series

NIH IRB Expectations for Return of Secondary Genomic Findings to Research Participants

OHSRP Education Series

Re-consent and Subject Notification: Expectations and Flexibilities for Complying with the Common Rule

OHSRP Education Series

Overview: NIH Multi-Site Protocol Processes

Protocol Navigator Meeting

Electronic IRB (eIRB) System Demo and Change Considerations

OHSRP Education Series

The Informed Consent Process-The Good, the Bad & the Ugly

OHSRP Education Series

Investigational Devices: What you need to know and Sponsor and Investigator Responsibilities

OHSRP Education Series

Determining Whether Your Project Might Require an Exemption or IRB Review

NCI CCR Clinical Research Forum

Health Literacy Considerations for Clinical Trial Communication and Decision Making

OHSRP Education Series

Regulatory Considerations in Natural History Studies

OHSRP Education Series

OHSRP Town Hall

OHSRP Education Series