International Clinical Trials Registry Platform (ICTRP)

WHO ICTRP Registry Criteria

Technical Capacity

Primary Registries in the WHO Registry Network will:

  • Submit the WHO Trial Registration Data Set for all records on their registry, in English, to the Central Repository
  • Have access to a database that is used to store and manage the submitted data
    • Primary registries are not required to develop their own database. See the Data Providers section for more information
  • Be able to demonstrate that they have access to adequate information technology support
  • Have adequate security and other provisions against data corruption and loss