Revolutionizing Clinical Research

We eliminate the operational chaos of clinical trials by providing purpose-built tools that transform fragmented, manual processes, delivering real-time data visibility and control, behavioral incentives, and predictive analytics.

60+%
Reduced Manual Work
40+%
Better Data Quality
90+%
Data Completeness
24/7
Real-time Monitoring

Key Features

Every component designed to empower patients, doctors, and monitors and accelerate trial outcomes

Complete Patient Visibility

Doctors gain instant, comprehensive access to each patient's health data, diary entries, and trial progress through automated data flows and real-time updates

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Unified Monitoring Dashboard

CRAs gain complete visibility across multiple trials with real-time metrics, compliance tracking, and automated alerts for protocol deviations

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Gamified Adherence System

Voucher-based reward system with achievement streaks transforms patient engagement, directly addressing the industry's adherence crisis

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Automated Anomaly Detection

Intelligent monitoring algorithms flag unusual patterns, adverse events, and protocol deviations instantly, enabling proactive intervention

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Seamless EDC Integration

Automated synchronization with global EDC platforms eliminates manual data reconciliation while maintaining enterprise-grade security and compliance

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Patient-Centric Mobile Platform

Comprehensive mobile experience for effortless daily logging, symptom reporting, medication tracking, and instant communication with clinical teams

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THE COST OF INEFFICIENCY IN CLINICAL TRIALS

Operational fragmentation creates cascading costs that delay life-saving treatments and inflate trial budgets

$300B+
Added Medical Costs
Annual healthcare burden from medication non‑adherence
50%
Patient Non-Adherence
Leading cause of preventable data loss
90%
Drug Candidates Fail
And each approved drug costs ~$2.6B to develop
$8M
Daily Loss
Trial delays cost sponsors $600K–$8M per day
Individual stakeholders' struggles do not just slow trials - they destroy them

Each broken link compounds the problem, driving up costs and failure rates. But there's a solution.

Connecting the Missing Links

Medify addresses the operational fragmentation that delays clinical trials by unifying patient data collection, investigator workflows, and monitor oversight in one platform. Explore the custom-tailored solutions for each key stakeholder below.

For Doctors

Instant Access & Streamlined Workflow

Medify gives doctors instant, secure access to each patient's data through automated data flows and built-in integrations with trial-critical systems.

Instantly enroll patients – one-time codes make onboarding fast and error-free

Complete visibility over each patient – view up-to-date health records and daily notebooks in one place

Automated alerts & notifications – be notified of adverse events or missing data so nothing critical goes unnoticed

Cross-systems integration – automatic syncing with global EDC platforms, which will eliminate copy-paste work

Doctor Interface

About Medify

Our Journey

MAR 2024

Founded

Medify was created to address the fragmentation, low data qualirt, and outdated processes slow down clinical trials across Eastern Europe. We set out to build technology that finally closes these gaps.

MID 2024

Strategic Pivot

After industry interviews and early testing, we expanded beyond medication adherence and evolved into a unified clinical trial platform—aiming to solve workflow inefficiencies at scale, not just at the patient level.

NOW

Validated & Testing

Our direction was validated in JA Bulgaria’s Beyond Pre‑accelerator, and we are now testing our late‑stage MVP with real clinical sites. The platform includes proper European localization, offline-first capabilities, and end-to-end regulatory compliance.

Get in Touch

Ready to revolutionize your clinical trials? Let's talk about how Medify can help.