Trials are conducted in participating sites. You must provide information about the site itself (organization), the investigator(s), and primary contacts (if a central contact is not provided). Optionally, you can include contact information for a person’s title (functional role) rather than a person’s name. When you add a participating site to a trial, link (associate) an organization, site, investigator(s), and primary site contact information to it.
Providing a site contact is optional if you provide a central contact instead.
The system assigns investigators and primary contacts a status code that corresponds to the person’s/role’s curation status.
Information about participating sites can be included in the protocol document or in the Participating Sites document.
