Clinical Trials

Allows for virtual clinical trial monitoring and management.

Integrates seamlessly with the healthcare organization’s EHR by utilizing the existing API and shares the pertinent information unidirectional or bidirectionally between systems in real-time and/ or provide a copy of the CCD file back to the healthcare organization’s EHR.

Provides delegation logs for the study coordinator (RNs), Principal Investigator (Physician), and Sub Investigator (Physician).

Virtual and scheduling abilities allow a patient to schedule a convenient time for the next visit in the comfort of their home or break from work.

Patient has the abilities participate in a clinical trial where and when they want without risking getting sick by visiting a health care organization.

Improved convenience and patient safety attracts new clinical trial study participants more quickly to start the clinical trial phases sooner.

The time it takes a compliance team member to review the information for submission can be reduced to as little as a couple of hours instead of 5 days due to the efficiency our solution offers.

Increased efficiency with our solution leads to cost reduction to complete a clinical trial.

Our seamless solution helps avoid room for human error eliminating the amount of manual entry which also reduces costs an improves safety.

Patient wearable information can be imported in the patient chart and clinical trial solution and monitored along with any reportable symptoms experienced by the patient.

CRA Services available if needed for additional support