ClinRegs is an online database of country-specific clinical research regulatory information designed to assist in planning and implementing international clinical research.

More information about this resource is available at ClinRegs

Main Areas of Focus

ClinRegs provides country-specific regulatory information in the following topic areas:

  • Regulatory Authority
  • Ethics Committee
  • Clinical Trial Lifecycle
  • Sponsorship
  • Informed Consent
  • Investigational Products
  • Specimens


  • Database of country-specific clinical research regulatory information

Who Can Use This Resource

  • Available for public use

How To Get Started

  • Go the ClinRegs website

Assurance to Requestors

Although ClinRegs contains information of a legal nature, it is intended for informational purposes only. It does not constitute legal advice or opinions as to the current operative laws, regulations, or guidelines of any jurisdiction, including the United States. 

Contact Information