Regulatory and Ethical Database (RED)
RED: Your Central Resource for Navigating the Clinical Study Regulatory & Ethical Submissions Requirements in Europe
Sailing through regulatory hurdles is one of the toughest challenges in multinational clinical research – The Regulatory and Ethical Database (RED) is here to clear the path and give your research the tools to cross borders.
With this tool, you can find the relevant information to support your clinical research for various study types: Investigational Medicinal Product, Medicinal Device, and Other (for observational studies, cohort studies, etc). The results are available for a range of European countries. Instead of looking into countries one at a time, you may also compare two directly.
How to use the tool?
RED is your go-to platform for comprehensive information on clinical study regulatory and ethical submission requirements across Europe.
Whether you're preparing a proposal for a multi-country study or expanding an ongoing study outside national boundaries, RED ensures you have precise, up-to-date information to guide your research application.
Key features:
- Tool navigation: select the country of interest, a study type, and a specific population (if desired) to access detailed information corresponding to your needs.
- Content overview: browse over 750 fields of detailed information, ensuring compliance and helping you make informed decisions for study submission.
- Compare regulations: effortlessly compare the regulatory and ethical requirements between different European countries for a given study type.
All of this is available with a user-friendly interface, regularly updated content from local experts, and designed to provide you with everything you need to plan, expand, or adapt your clinical studies confidently.
Watch our demo video now and discover how to navigate Europe’s clinical research landscape like a pro!