OHSP Feedback Form
Seminar Materials
The “Business” of Clinical Research – How to Conduct Trials Efficiently and Ethically - December 13, 2011
The Unique Human Subjects Considerations for Various Kinds of Genetic Research, Including Genetic Testing - October 11, 2011
Conducting Human Subject Research at the UR: Writing and Implementing Research - September 22, 2011
- Agenda - Conducting Human Research Workshop
- Protocol & Investigator Responsibilities
- Informed Consent: Federal Regulations, Institutional Policy & Good Practice
- Study Approval: What's Next?
Understand the Basics of Genetic Testing - July 27, 2011
Conducting Human Subject Research at the UR: Writing and Implementing Research - April 11, 2011
- Agenda - Conducting Human Research Workshop
- Handouts - Conducting Human Research Workshop
- Protocol Training Presentation
- Protocol Template
- Informed Consent Presentation
- Protocol Deviations Presentation
- Reportable Events Presentation
- Documentation/PI Oversight Source/Documents Presentation
Understand the OHSP QI Process and Improving the Research Process - March 8, 2011
Preparing to go online with WIRB: Training and Guidance - February 15, 2011
Informed Consent: Federal Regulations, Institutional Policy & Good Practice - January 25, 2011 - Video of presentation
Reportable Events 2010 - March 16, 2010
RSRB 101: Structure, Activity and Update - February 9, 2010
Protecting the Rights and Safety and Welfare of Subjects Supervisory Responsibilities of Investigators - September 8, 2010
Innovation at a Crossroads: Economic and Political Perspectives on the Drug Development Process - June 16, 2010