Regulatory Specialists
Receive regulatory guidance and support for your clinical trial.
How we can help
- Navigate the IRB submission process.
- Maintain your study documents and regulatory binder.
- Reduce the number of common stipulations on your IRB submissions.
- Ensure your study files follow Good Clinical Practice guidelines.
- Discover other useful resources for your study.
Support options
Cost
Consult with an expert
Sydney Viel
Regulatory Affairs Program Manager
[email protected]
Melissa Hansen
Research Navigator
[email protected]
612-625-CTSI (2874)