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| Date |
Time |
| Mon 12/10/2018 |
02:30pm - 04:00pm |
Learning objectives of this interactive workshop include:
1. To describe required IRB communications for study reporting (including for reliance/single IRB), protocol amendments, and participant re-consenting
2. To identify applicable institutional clinical research SOPs and IRB working policies and procedures
3. To apply best practices for IRB communication pathways through the use of scenarios
Prerequisites: Please bring ID (for attendance log-in) and laptop (if convenient - not necessary, but may be useful)
- Cost:
- $0.00
- Sponsor:
- Clinical and Translational Research
- Audience:
- VCU Faculty and Staff Only
- Category:
- Clinical Research, Professional Development, Teaching/Learning
- Contact:
- Helm, Shirley L
804-628-2942
shelm@vcu.edu