🗃️ Data Capture
Day-to-day data capture: the study dashboard, subjects, visits, data entry and the AI data entry assistant.
🗃️ Data Compliance
Protect and trace study data: PHI management and the study audit logs.
🗃️ Extract Data
Get data out of the study as casebooks and datasets.
🗃️ Randomization
Use the Randomization workspace's 6 tabs — Dashboard, Subjects, Requests, Randomization Codes, Tools, Export — during study operations.
🗃️ IMP Operations
Manage investigational medicinal product (IMP) supply while the study runs, for PSP and randomization studies, plus IMP reports.
🗃️ Pre-Screen & eConsent
Run pre-screening and electronic consent with subjects: overview, step-by-step user guide and role-based SOP.
🗃️ Queries
Raise, answer and close data queries during the study.
🗃️ SDV
Source data verification: what SDV covers, how to verify data and who does what.
📄️ Medical Coding
Use the Medical Coding app to review, search, and assign standardized medical codes to verbatim terms collected in CRFs, and manage reusable aliases for recurring terms.
🗃️ Monitoring Visit
Plan, run and report site monitoring visits: overview, user guide and role-based SOP.
📄️ e-Signature
Use Signature to sign subject records in the study workspace, including review, credential confirmation, and signed status tracking.
📄️ CDS Surveys
Use the CDS Surveys workspace to monitor participant survey assignments, manage participant groups, and configure survey packages for email delivery.
🗃️ cds-surveys
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🗃️ medical-coding
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