NIH Human Subject Compliance: Are You Including the Right Populations?

60 Minute On-Demand Webinar. Available in CD, MP4 or PDF Transcript

This Webinar is a part of the “NIH Grant Application 10-Part Webinar Series.” Click here to learn more!

or Call 1-800-303-0129 ext. 506

If your proposal involves human subjects, you must upload several separate documents indicating who will be involved, why and how they will be impacted. Consequently, you’ll need to thoroughly understand the regulatory and ethical issues associated with human subjects, as well as institutional review board (IRB) processes. Additionally, you will have to consider NIH’s position on including of women, minorities and children in your project.

From this insightful webinar, your will walk away with actionable next steps to make sure you will conduct your research according to all the applicable rules. And you will have the tools to ensure your proposal includes the appropriate details so reviewers will have no questions about what you intend to do.

5 Key Take-Aways:

  • A thorough understanding of exempt categories
  • Recognizing the IRB’s role in reviewing the research protocol and proposal
  • The importance of equitable subject selection and its historical underpinnings
  • What IRBs may be looking for when examining your project
  • Understand NIH’s human subject compliance resources

Limited-Time Offer!

  • CD-ROM with PDF Handouts — Reg. Price: $197 Now: Only $99!
  • MP4 with PDF Handouts — Reg. Price: $197 Now: Only $99!
  • PDF Transcript with Handouts — Reg. Price: $197 Now: Only $99!

 Meet Your Presenter:

Jaime A. Arango, Ed.D., CIP serves as the Assistant Director of Education for Human Subjects Protection at the Collaborative Institution Training Initiative (CITI) Program at the University of Miami and is a Certified IRB Professional. Prior to joining CITI, Dr. Arango was the Director for Human Subjects Protections/IRB at Nova Southeastern University. In that capacity, he oversaw the operations of the NSU IRB including the initial and continuing review of research protocols involving human subjects, many of which were funded by the NIH. Dr. Arango has worked with IRBs since 2002. He also currently serves as a community member for the Florida Department of Health IRB and as a mentor through the Public Responsibility in Medicine and Research (PRIM&R) organization.


This Webinar presentation is brought to you as a training tool by the Principal Investigators Association, which is an independent organization. The presentation, tools presented and their contents are not connected with the National Institutes of Health (NIH), nor are they endorsed by this agency. All views expressed are those personally held by the presenter and are not official government policies or opinions.