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

e TMF

Remote monitoring / remote source data verification

Query resolution

Data analytics

Access studies

Study agreements

Scan/upload source documents

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

Monitor stock real-time by subject

Access studies

Check inclusion & exclusion criteria

e-Consent with investigator confirmation

Direct data capture with point of care devices

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..)