Showing results for IRB

FERPA: A Quick Review of the Law for Researchers and IRBs
Presented by: Thomas Gold, PhD - Acceleration Group, Inc. This webinar explores the Family Educational Rights and Privacy Act (FERPA) (20 U.S.C. ...
Single Institutional Review Board (sIRB) Use and Administration: Authorization Agreements
Introduces best practices for drafting, reviewing, and implementing authorization agreements between the sIRB and participating sites in multi-site re...
HRPP/IRB Policies and Procedures
Provides learners with an understanding of both the requirements and best practices for IRB written procedures, procedure development and content, tec...
Race in Clinical Research: Ethics and IRB Decision Making
Presented by: Nicolle Strand, JD, MBE, MPH - Lewis Katz School of Medicine, Temple University Learning Objectives: Explain why race should...
HRPP/IRB Policies and Procedures
Provides learners with an understanding of both the requirements and best practices for IRB written procedures, procedure development and content, tec...
What Are IRBs?
This module explains the purpose of and membership requirements for IRBs.
Working with IRBs, Compliance Committees, and Regulators
The module details clinical research regulations and the oversight of research. It explains the role of an Institutional Review Board (IRB), complianc...
All Access Webinar Package (Organizations Only)
The All Access Webinar Package includes all of CITI Program’s currently available webinar recordings as well as future recordings released during yo...
Participatory Science and the Institutional Review Board
Participatory science—research conducted with or by members of the public—offers powerful opportunities for collaboration, innovation, and communi...
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