Care and Trial Site Registry (CTSR) helps clinical investigators select trial sites as well as to help to identify potential partners for upcoming research projects.Visit website
Clinical Research Metadata Repository (including COVID-19 data), allowing researchers to access clinical studies and related data objects. These include, for example, protocols, information sheets and consent forms, data management plans, statistical analysis plans, case report forms, results, publications, descriptive metadata, etc. MDR contributes to making clinical research data from all disease areas FAIR by increasing data Findability. Browse and search metadata on clinical trials—as well as all related documents
FAIRsharing.org (standards, databases, policies) is a place to discover standards, repositories and data policies and how they interlink. It also features a prototype educational page on standards. The resource serves all disciplines and has been adopted by funders, publishers, RDA and other organisations.