• Does your human subjects research qualify as a clinical trial according to NIH, subject to the same reporting requirements in ClinicalTrials.gov?
  • Is it time to report your clinical trial's progress to a funding organization?
  • Is your trial being audited by FDA or IRB?

Expert Guidance

Our CRSP regulatory team can help you decipher and successfully meet your study's reporting obligations, whether for NIH ClinicalTrials.gov, in response to an FDA audit, or as part of an internal IRB review. 

Fees

Access a list of CRSP fees here (BlazerID & login required). 

Register

To register for a CRSP service, please fill in a CCTS Clinical Services form and submit it to This email address is being protected from spambots. You need JavaScript enabled to view it..

Don't see what you need? Have an urgent request? Contact us at This email address is being protected from spambots. You need JavaScript enabled to view it. or 205-934-7442.