Medication Adherence Monitoring Software

Innovative Medication Adherence Solutions for Real-Time Monitoring and Tracking. Ensuring Medication Adherence in Clinical Trials

Accurate medication adherence is essential for clinical trial success. Non-adherence can distort data and prevent researchers from assessing the true effectiveness of treatments. Med-Con Mobile’s AI-powered solutions are designed to address this challenge in pharmaceutical research and clinical trials.

Real-Time Medication Adherence Tracking

Med-Con’s smartphone app, combined with unique 2D bar codes on medication packaging, makes it easy to track each participant’s dosing activity. All doses are monitored in real-time via secure wireless technology, with data instantly accessible through a cloud-based server. This provides full transparency for clinical teams to act quickly and address any issues.

If a participant misses or delays a dose, the trial team receives alerts, allowing for patient engagement to help the subject stay on schedule. This ensures better adherence and supports the success of your study.

How Med-Con’s Mobile App and Smart Labels Improve Adherence

Med-Con’s solution addresses common barriers to medication adherence in outpatient clinical trials. With reminders and real-time alerts, it ensures participants are prompted to stay on track with their dosing regimen. Key features include:

• Dose reminders when it’s time to take medication.
• Real-time alerts for missed or late doses, allowing for site staff intervention.
• Our web portal offers secure access to detailed, time-stamped reports on each subject's dosing history, along with a comprehensive summary of adherence for the entire study.

These tools empower you to make more informed decisions that can enhance study success, outcomes, and cost-efficiency.

Maximizing Study Outcomes with Med-Con’s Adherence Technology

Our software tracks adherence and provides reports that give accurate insight into each participant's dosing behavior. Investigators can review these detailed reports via our web portal to monitor dosing and improve adherence (via patient engagement). This ensures participants closely follow their prescribed regimens. This allows for both improved adherence and enhanced data accuracy, helping studies to meet primary safety and efficacy endpoints.