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Audience
This guide is for trial designers, developers, and administrators such as:
- Clinical Data Managers (CDMs) and other trial design personnel who:
- Design and implement electronic Case Record Forms (CRFs).
- Specify automated data edit checks.
- Manage libraries of trial definition components such as forms and edit checks.
- Design electronic trial documentation, including protocols and CRF help.
- Application Engineers (AEs) and other trial development personnel who:
- Develop and apply automated edit checks.
- Design and implement custom databases for downloading trial data.
- Develop custom reports.
- Implement electronic trial documentation.
- Help desk and other administrative personnel who:
- Set up and maintain users, sites, rights, and groups.
- Set trial-wide configuration options.
