User Management
- Create Sites remotely and e-sign Investigator's agreement
- Role based creation of Users for Sponsors & Site staff
Study Management
- Seamless Integration with Existing Systems & Applications to build Front End Modules (Handheld, Mob and Tabs)
- Management of multiple studies on single Dashboard
- Real Time Information of Study Progress, Data Outliers, AE’s & SAE’s
- Real time drug performance through e-PRO / e-COA
- Automated Data Management Process to capture quality data and reduce query management time
Clinical Operations
- e-TMF
- Remote Monitoring / Remote Source Data Verification
- Query Resolution
Report Analytics
- Monitor Study Wise Users
- Visit Wise Reports
- Location Wise Users
Study Management
- Access Studies
- Study Agreements
- Scan/Upload Source Documents
- Query Resolution
Patient Management
- Enrolling Participants
- Inclusion & Exclusion Criteria with e-Consent
- Patient Randomization
- Access Electronic Based CRF
- Subject Medication Monitoring through e- PRO
- Monitoring & Interacting with Subjects through Tele-Medicine
- Access Electronic Based CRF and respond to queries
- Monitor AE’s & SAE’s real time
- Participant Dairy Access
- Integrated with Apple Watch for Realtime Health
Study Management
- Access Studies
- Consent with Investigator Confirmation
- Direct Data Capture with Point of Care Devices
Participant Management
- Access Electronic Based CRF & e-PRO
- Participant Dairy Access
- Add Adverse Events/ Serious Adverse Events
- Investigator communication Access on every Stage using Tele-Medicine
- Alerts & Notifications for Medications
- Real Time Drug Stock Information & Management
- Integrate with Point of Care Devices for Drug performance & Health progress (Smart Watch, Glucometer, etc..)
