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AUTOMATE TRIALS · FOR PHARMA

Real-world AI data, on the timeline you have.

Automate Trials is the pharma and life-sciences surface on the Automate Medical platform — real-world data, trial operations, safety, and RWE, all on the same trust layer as the patient and provider experience.

Automate Trials
1.8×
Improvement vs baseline
FDA-aligned
Compliance reporting
Dedicated
Pharma CSM
Features

What Automate Trials does.

Site selection + eligibility enrichment

Real-world data feeds for site feasibility, investigator scoring, and eligibility enrichment that reflects the actual patient population.

Trial-operations AI

Operational analytics on enrollment, retention, and protocol deviations — surfaced before they become a study-level problem.

DSMB and safety dashboards

Continuous safety signal monitoring with audit-logged access for the data safety monitoring board.

Investigator scoring + risk flags

Score and rank investigators on historical enrollment, retention, and data quality — with risk flags when signals shift.

Compliance reporting (FDA-aligned)

Structured outputs aligned to FDA reporting requirements. Submission-ready.

Dedicated pharma CSM

Every Automate Trials plan includes a dedicated customer success manager with pharma experience.

Compress the timeline.

Real-world AI data, on the timeline you actually have. Talk to the Automate Medical pharma team.

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