Frequently Asked Questions

Frequently asked questions

Some additional information about MedMonitor's technology and process.

How does MedMonitor work?

The core of MedMonitor is our proprietary clinical rules made up of 1,700+ algorithms. These rules are kept up-to-date with new drug information and treatment guidelines. All the alerts are manually designed, validated, and regression-tested.

How do you ensure data privacy and security?

MedMonitor is a closed-loop AI system with predictable outputs. All alert logic is manually designed, clinically validated, and regression-tested before deployment. Security includes network segmentation, encryption, IP restrictions, and identity/access management.

What types of medication issues does MedMonitor identify?

MedMonitor flags five categories:

  • Gaps in care: Missing medications, wrong drug choices
  • Adherence: Not refilling meds, therapy drop-off
  • Safety: Inappropriate dosages, duplicate therapy, inappropriate medication use in elderly populations, drug interactions
  • Screening: Screening to capture long-term effects of medication use in specific circumstances such as mental illness
  • Cost savings: Ensuring therapeutic substitutions and dosing combinations are optimized and capturing other plan-specific opportunities to save costs

Will this disrupt our relationship with healthcare providers?

No. MedMonitor supports healthcare teams by running in the background. It flags issues when medications change, dosages adjust, or guidelines update. Communications are targeted: providers get detailed clinical information, members get simplified guidance. Pharmacists vet all alerts, keeping healthcare providers central to care decisions.

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Find out how MedMonitor can reduce costs and improve health outcomes.
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