At your request, at a location and time convenient to you, OHRPP senior staff will customize workshops to suit the needs of your faculty, staff and students. Some examples of topics are listed below:
- General Introduction: Human Subjects Research
- Tips for Speeding Up IRB Approval
- webIRB: Successfully Preparing a Full Committee Review Application
- webIRB: Successfully Preparing an Application for Exempt Certification
- Post Approval Event Reporting (Adverse Events, Incidents, Violations)
- Preparing Consent and Assent Forms
- The Consent Process
- Research Using Human Biological Specimens
- Research Involving Children
- Conducting Research in an International Setting
- Investigational Drugs and/or Devices in Research
- Good Clinical Practice (GCP) Training
Request Training or Presentations
Call (310) 206-2040 or email the OHRPP Quality Improvement and Education Unit to discuss your needs.
Page Last Updated: May 4, 2021