Regulatory Specialists


Receive regulatory guidance and support for your clinical trial.

Request support

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


Consult with an expert

Sydney Viel
Regulatory Affairs Program Manager
[email protected]

Melissa Hansen
Research Navigator
[email protected]
612-625-CTSI (2874)