The ClinRegs resource is an online database of country-specific clinical research regulatory information designed to allow users to explore regulations within a country and compare requirements across countries. By providing well-documented, up-to-date regulatory information for multiple countries in a single place, ClinRegs is intended to serve as a central resource and time-saver for individuals involved in planning and implementing international clinical research.ClinRegs‘ interface is easy-to-navigate and enables users to obtain a digestible overview of a country’s regulatory requirements related to a specific topic. Additionally, ClinRegs provides links to official regulations and other key resources related to international clinical research.
ClinRegs provides an overview of country-specific regulations in the following topic areas:
- Competent Authority Oversight
- Ethics Committee Oversight
- Clinical Trial Lifecycle
- Sponsorship
- Informed Consent
- Investigational Products
- Specimens