Sponsor

  • Create sites remotely and e-sign investigator's agreement
  • Role based creation of users for sponsors & site staff
  • 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

Site

  • Access studies
  • Study agreements
  • Scan/upload source documents
  • Query resolution
  • Enrol subjects remotely
  • Inclusion & exclusion criteria with e-Consent
  • 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 data

Subject

  • Access studies
  • Check inclusion & exclusion criteria
  • e-Consent with investigator confirmation
  • Direct data capture with point of care devices
  • Access studies
  • Access electronic based CRF & e-PRO
  • 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..)