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Training on Human Subjects Protections: Part 3HHS Only

Air date: Thursday, June 2, 2011, 9:00:00 AM
Time displayed is Eastern Time, Washington DC Local
Description: WHO SHOULD ATTEND?

Scientific Review Officers, Program Officers, and Grants Management staff who are new to NIH, or new to human subjects research administration Other NIH extramural staff who want a refresher on human research protections

NOT SURE? CAN YOU CORRECTLY ANSWER THE FOLLOWING QUESTIONS
  • A study involves the use of specimens from cadavers plus identifiable clinical information retrieved from their medical records – is this human subjects research?

  • Reviewers identify concerns with the proposed plan to recruit minorities in an application. Should this application also be coded as unacceptable for human subjects?

  • NIH has determined that a particular study is not considered human subjects research. However, the PI's institutional IRB wants it to undergo review. Should NIH staff tell the Institution that IRB review is not necessary?

  • What is the appropriate human subjects code for this grant?
IF NOT, THEN YOU SHOULD ATTEND THE DECEMBER 2ND TRAINING!!

Sessions II and III will be held on March 10, 2011 and June 2, 2011 in RK-2, rm 9112-9116 and will cover timely topics such as use of existing specimens. Details about these training sessions will be sent via email and posted on the web page listed below.

http://esa.nih.gov/oer/training/esa/esa_training_20101202.htm
Author: Ann Hardy and Maria Stagnitto
Runtime: 2 hours