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Every module on the ClinicalDataS platform, grouped by what it does.
Form BuilderDesign & version eCRFs.SDVSource data verification.QueriesRaise & resolve data queries.RandomizationRTSM / IWRS allocation.IMP SupplyInventory, dispense, reconcile.Medical CodingMedDRA / WHO Drug coding.Monitoring VisitPlan visits, log findings, CAPA.e-SignatureSign at form & subject level.Pre-Screen & eConsentRecruit & consent participants.Casebook & eTMFe-Source & trial master file.Rule StudioBuild validation & calculation rules.CDS SurveysPatient-reported outcomes & surveys.
Trust & Compliance
Built for regulated clinical research
Understand how CDS protects patient data and meets the standards your sponsors and auditors expect.
21 CFR Part 11e-signatures & audit trail
GDPREU data protection
Nghị định 13/2023Vietnam personal data
PHI Managementmasking & access control
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What's new
04 Jun 2026
AE/SAE — ICSR module launched
22 May 2026
Vietnamese (VI) docs now available
10 May 2026
Rule Studio: new formula editor
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