ClinRegs is an online database of country-specific clinical research regulatory information designed to assist in planning and implementing international clinical research. By providing well-documented and current information in a single place, ClinRegs serves as a central resource and time-saver for those involved in clinical research.
Past Event
Check out a replay of our May 23, 2024 webinar:
Utilizing NIAID’s ClinRegs Website to Support International Clinical Research Regulatory Compliance
The webinar provides background on the site, a demo that highlights the site functionality and navigation, details on how the information is kept-up-to date, current usage trends, and how to stay engaged.
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
Tools
- Links to official requirements and other sources, including English translations when available
- On-page notifications about recent changes to country requirements
- Side-by-side view of up to four country profiles
- Keyword search
- Feedback mechanism in each country profile section
- Sharing mechanism in each country profile section
- Updates page highlighting revisions to country profiles
Who Can Use This Resource
- Available for public use
How To Get Started
- Go to the ClinRegs website
- Sign up for topic or country specific regulatory updates
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.