The following presentations are from the informational sessions that have been presented by the OHSR Compliance Monitors. To date, these presentations have highlighted organization and conduct issues observed from site visits. Also included in these presentations are practical recommendations to implement strategies to increase regulatory and subject compliance, as well as helping with the preparation for monitoring and audit visits
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| Dates for Upcoming Seminars: |
Bayview Campus
Carroll Auditorium
Monday, March 10, 2008 10AM-11AM - “The Research Protocol from Approval through Termination: Monitoring Implications”
Monday, September 22, 2008 10AM-11AM |
East Baltimore Campus
Broadway Research Building, G01 & G03
Tuesday, March 11, 2008 10AM-11AM - “The Research Protocol from Approval through Termination: Monitoring Implications”
Tuesday, September 23, 2008 10AM-11AM
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| Previous Seminars: |
"Audit Preparation Suggestions and Strategies" - Spring 2006 |
"Projects That Do Not Involve FDA Regulated Products: Investigator Responsibilities and Compliance" - Fall 2006 |
"Common Informed Consent Problems and Solutions" - Spring 2007 |
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