Pharma Clinical Trial Automation

Accelerate trial screening. Convert unstructured patient histories, lab reports, and medication logs into standardized clinical trial datasets.

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Current Challenges

Sifting through pages of clinical histories manually to verify patient trial eligibility.
Normalizing raw study documentation to standard medical terminologies is high overhead.
Ensuring data compliance logs meet FDA and regulatory security requirements.

The MedIngest Solution

AI parses and classifies clinical records, highlighting key exclusion findings.
Extracted medication names are mapped directly to RxNorm and drug databases.
HIPAA-compliant security framework with detailed system audit records.

Integration Workflow

Our automated ingestion workflows interface natively with your existing EHR and file networks.

Study Intake

Raw patient history PDFs are uploaded to the clinical trial database.

Map & Normalize

AI parses findings and matches medications and codes to RxNorm.

Trial Data Sync

Structured parameters are pushed to the clinical research repository.

Proven Return on Investment

Trial Screening

Increase in patient trial eligibility evaluation speeds.

80%

Mapping Time Saved

Reduction in manual medical terminology coding tasks.

Compliance Risk

All patient data processed complies with standard audit protocols.

Customer Outcomes & Success Metrics

Accelerated Trials

Screen patients faster, decreasing trial setup timelines.

Terminology Links

Ensures uniform drug displays by mapping text to standard RxNorm codes.

Data Integrity

FDA-compliant database audits with complete document access logging.

Ready to Accelerate Your Workflows?

Schedule a technical demonstration with our healthcare integration architects to evaluate your ingestion setups.

Request a Demo