DocEX

Clinical Research Data Structuring

Life Sciences Document Processing | Pharma / Biotech

The Challenge

 

Client maintained 10+ years of clinical trial data in scattered, unformatted Excel files with no standardization, inconsistent definitions, and poor regulatory readiness.

Manual processing took weeks and error rates were high (8–12%).

Solution: DocEX

 

AI-driven NER + ontology-based data extraction engine converting raw research into regulatory-ready structured formats.

Core Capabilities

Clinical NERAuto-extract dosages, demographics, efficacy %, study methods

Ontology MappingLink entities to RxNorm, SNOMED-CT, MedDRA

Study Outcome MatrixBuild structured outcome tables per trial

Ingredient-Condition MappingGenerate formulation recommendations based on clinical evidence

AI / ML Components

Named Entity RecognitionExtract clinical terms, dosages, and demographics

Ontology MatchingMap extracted data to standardized medical taxonomies

Study Outcome MatrixStructured clinical data compilation

Efficacy ScoringEvidence-based formulation recommendations

Deliverables

 
  • Standardized Excel + JSON repositories with normalized schema
  • Research-backed formulation recommendations with dosage ranges
  • Traceability with confidence scores per extracted field

Business Impact

 
MetricBeforeAfterImprovement
Doc Cycle15–20 days2–3 days85% faster
Data Entry Errors8–12%<0.5%99% reduction
Regulatory PrepWeeks of rework3–5 days readyAudit-ready
R&D Iteration2–3 weeks3–4 days80% faster

 

Key Outcomes

✓ 85% faster documentation cycles
✓ Regulatory-submission ready structures
✓ Strong proof base for compliance positioning
✓ Scalable formulation decision-making

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