e-Recruitment: Screen & enrol patients remotely
e-PRO: Connect & follow up with patients for outcomes
e-COA: Monitor clinical outcomes from point of care devices / wearables
e-TMF: Manage trial master files in electronic or digital format
e-Source: Direct data capture of CRF, lab and medical history on realtime basis
Digital consent of the patient with regulatory compliance
Tele visits: Engage & communicate with patients seamlessly
End to End Services as a functional service provider (protocol, EC, CTA, site onboarding, mobile based data capture, analysis & manuscript publishing)
AI enabled & automated protocol writing, clinical trial agreement, site onboarding, automated validation/verification of source documents, analysis, CSR & manuscript writing
Study set up in 15 days for EDC studies
Mobile based e-Consent & e-PRO (customized for each study)
Automated e-CRF with CDISC & SDTM mapping
Integrated forms with embedded algorithms
Remote monitoring / RSDV / risk based monitoring
Integrated randomization module
AI enabled risk based monitoring
Project management with real time data & analytics
Portal for patients for participating in clinical trials with consent (e Recruitment)
Clinical supplies inventory management application
Build SDTM/CDISC/ADaM data structures
Mobile apps for HCPs & patients by therapeutic area
Cloud infra management with front end modules
Develop custom made applications
