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Welcome
ClinRegs is an online database of country-specific clinical research regulatory information designed to assist in planning and implementing international clinical research. Countries are included based on NIAID's international clinical research priorities. For additional information, see the About page.
If a country you are looking for is not included in ClinRegs, consider the following resources:
- HHS OHRP’s International Compilation of Human Research Standards
- European Clinical Research Infrastructure Network’s CAMPUS for Regulatory and Ethical Requirements
For questions or comments, please click on Contact Us at the top of the page or take our Feedback Survey.
Check out the ClinRegs fact sheet and share it with your colleagues!
Updates
ClinRegs Functionality Upgrades
May 3, 2024 - To provide a better user experience and make information easier to find, we have made the following improvements to ClinRegs:Country pages now include tabular dashboard and topic filterSearch results page now includes option to view results for up to 4 countries side-by-sideFor additional details, ...
Australia Profile Updated
May 2, 2024 - The Australia profile in ClinRegs has been reviewed and updated with the following information:Revised National Health and Medical Research Council (NHMRC) guidance on ethics committee requirements and research governance responsibilities of institutions (See the Ethics Committee topic, Submission ...
Peru Profile Updated
Apr 24, 2024 - The Peru profile in ClinRegs has been reviewed and updated with the following information:Legislative decree from 2018 modifying Peru’s research center registration certificate requirements (See Timeline of Review)October 2023 National Institute of Health (Instituto Nacional de Salud (INS)) ...
Thailand Profile Updated
Mar 21, 2024 - The Thailand profile in ClinRegs has been reviewed and updated with the following information:Revised requirements and documentation for importing drugs for clinical research (See the Regulatory Authority, Ethics Committee, Clinical Trial Lifecycle, Sponsorship, Informed Consent, and Investigational ...