What's new
- Sign and verify data in a study
Principal investigators can now sign data at a subject level and Clinical Research Associates (CRAs) can now verify data to make sure the information collected in a study is accurate. - Add customized fields to the Subject Events report
Clinical Research Associates (CRAs), data managers, study managers, lead site users, and site users can now customize their Subject Events report with specific fields. - Send kit replacement and kit re-dispensation data to Oracle InForm
Integration managers can now send more data about additional kit-related events from Oracle Clinical One Platform to Oracle InForm.