Decentralized clinical trials
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
e-Consent: Digital consent of the patient with regulatory compliance
Tele visits: Engage & communicate with patients seamlessly
Seamless onboarding of investigators & patients
Electronic data capture
CTMS/RBMS/Remote monitoring/project management
IWRS
Clinical supplies inventory management
Real world observational studies
Execute investigator initiated study, registry study, real world retrospective / prospective study,
post marketing surveillance studies seamlessly
Integration with point of care devices for direct data capture
Realtime clinical outcome assessments & analytics
Automated data entry, data collection & validation / verification of source documents
Real time monitoring of AE’s & SAE’s through alerts & notifications
Redact patient sensitive data in the app itself and review the source data along with query management
AI based advanced search on documents/files
Automation of trial design, study protocols & CSR’s
Descriptive, predictive, prescriptive analysis of clinical trial data
