A well-written clinical research protocol is critical to successful study execution, regulatory compliance, participant protection, and data integrity. ICTR provides consultative and “pen-to-paper” protocol development support with the goal of improving the quality of investigator-initiated clinical research and reducing the time from study conception to conduct.
Complimentary services are available to faculty planning an investigator-initiated clinical research study (non-therapeutic or therapeutic):
- Guidance on study design
- Assistance writing and editing clinical research protocols
- Development of UW-specific protocol templates that fulfill Institutional Review Board (IRB) requirements