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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
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 ...
Tanzania Profile Updated
Mar 1, 2024 - The Tanzania profile in ClinRegs has been reviewed and updated with the following information:Government of Tanzania law (effective May 2023) and regulations (effective July 2023) on personal data protection, including information on responsible parties, collection, processing, and consent ...
ClinRegs Functionality Upgrades
Feb 20, 2024 - To provide a better user experience and make information easier to find, we have made the following improvements to ClinRegs:Option to view up to 4 countries side-by-sideCountry pages now include:Section descriptionsMenu “Hide” option for easier viewing For additional details, please ...
Uganda Profile Updated
Feb 9, 2024 - The Uganda profile in ClinRegs has been reviewed and updated with the following information:New and updated guidelines on manufacturing, importing, and managing investigational products (See the Investigational Products topic)Additional details on requirements for clinical trial amendments ...