Supporting clinical trials across borders

The Adaptive Platform Trial Toolbox aims to collect the accumulated knowledge, experience, and resources (collectively termed as ‘tools’) from multiple projects and trials into a practical and guided toolbox to facilitate planning and conduct of future adaptive platform trials in any therapeutic area. 

The Clinical Research Metadata Repository is the free online tool to help scientific researchers find documents and data linked to a clinical research study, and to obtain information on the accessibility of those results.

The toolbox aims to collect the accumulated knowledge, experience, and resources generated by previous projects and/or research infrastructures and other organisations into a practical and guided toolbox to help understand the regulations and requirements for conducting trials, with special focus on investigator-initiated trials for rare diseases. 

A series of tools and procedures to support the setup and management of multinational neonatal and paediatric clinical trials in Europe were developed through the PedCRIN project.

The Risk-Based Monitoring Toolbox provides information on tools available for risk assessment, monitoring and study conduct, the institutions where they are used, and other relevant details such as links and user feedback.

ECRIN RED is a central resource for information about clinical trial regulatory and ethical requirements covering a number of European countries and multiple study types such as clinical drug trials, clinical investigations of medical devices, combination drug-device studies and nutritional studies.