For Pharma

Accelerate clinical development with real-world evidence

Accelerate clinical development with real-world evidence

Nimblemind transforms fragmented clinical and real-world data into structured, reliable datasets for faster cohort identification, study execution, and decision-making.

Pharma teams are slowed by manual, fragmented data workflows

Pharma teams are slowed by manual, fragmented data workflows

Manual data extraction is time-consuming

Real-world evidence requires manual chart abstraction from clinical notes, reports, and PDFs.

Data preparation costs are high

Per-patient data preparation can cost $1,200-$2,500, making it difficult to scale studies efficiently.

Long timelines delay study insights

Studies often take 9-18 months before datasets are ready, delaying analysis and decision-making.

Study scope is limited by constraints

Time and budget constraints restrict cohort sizes, limiting study scope and slowing evidence generation.

Our Solution

From fragmented clinical data to analysis-ready real-world evidence

From fragmented clinical data to analysis-ready real-world evidence

Nimblemind transforms unstructured clinical documentation into consistent, traceable datasets, enabling faster study execution and more reliable insights.

1

Extract clinical information

Identify variables like diagnoses, outcomes, treatments, and patient characteristics from unstructured clinical documentation.

2

Align to study definitions

Map extracted data to study protocols, cohort criteria, and endpoint definitions to ensure consistency across analyses.

2

Align to study definitions

Map extracted data to study protocols, cohort criteria, and endpoint definitions to ensure consistency across analyses.

3

Structure and prepare datasets

Generate standardized, analysis-ready datasets that support efficient cohort building and downstream research workflows.

4

Enable reuse across studies

Create structured data assets that can be reused across studies, reducing duplicate effort and accelerating future research.

4

Enable reuse across studies

Create structured data assets that can be reused across studies, reducing duplicate effort and accelerating future research.

Outcomes that prove it works

Outcomes that prove it works

Faster time to first dataset

Generate analysis-ready datasets in weeks instead of months, accelerating study start and downstream research timelines.

Faster time to first dataset

Generate analysis-ready datasets in weeks instead of months, accelerating study start and downstream research timelines.

Increase cohort size and study scale

Enable larger, more representative patient cohorts without increasing data preparation effort or cost.

Reduce manual data abstraction effort

Minimize time spent reviewing and extracting data from clinical documents, shifting teams toward analysis and validation.

Reduce manual data abstraction effort

Minimize time spent reviewing and extracting data from clinical documents, shifting teams toward analysis and validation.

Lower data preparation costs per patient

Reduce per-patient data prep costs by replacing manual abstraction with scalable, structured data pipelines.

Real-world deployments across clinical specialties

Real-world deployments across clinical specialties

Ophthalmology

Works with fundus imaging and clinical notes to generate consistent datasets for severity scoring, analysis, and clinical workflows.

Gastroenterology

Handles endoscopy video and clinical context to produce usable datasets for detection, evaluation, and downstream analysis.

Radiology

Supports radiology imaging across sources and formats, making it usable for analytics and model development.

Anatomical Pathology

Works with high-resolution pathology images to create structured datasets for analysis and deployment.

Data types supported in pharma data pipelines

Data types supported in pharma data pipelines

Nimblemind ingests and structures the data sources most critical to real-world evidence generation and clinical research workflows.

Modality

Examples

EMR and Clinical Notes

Diagnoses, symptoms, physician notes, discharge summaries, medications

Claims and Billing Data

Procedures, ICD/CPT codes, utilization patterns, longitudinal patient journeys

Lab and Biomarker Results

Blood panels, biomarkers, disease-specific lab values, longitudinal trends

Imaging and Diagnostics

Radiology reports, pathology reports, imaging summaries, diagnostics

Genomic and Molecular Data (where applicable)

Genetic variants, biomarker panels, pharmacogenomic profiles

Patient-Reported Outcomes (PROs)

Surveys, symptom diaries, quality-of-life assessments

Clinical Trial and Registry Data

Study records, cohort definitions, endpoints, observational registries

See how we support real-world evidence workflows

See how we support real-world evidence workflows

Book a call to explore how we help pharma teams prepare structured, labeled datasets with less effort and more control.

Nimblemind

Nimblemind offers a faster and safer way to structure, label, and manage multimodal health data with automation, audit trails, and APIs.

© 2026 Nimblemind. All rights reserved.

Nimblemind

Nimblemind offers a faster and safer way to structure, label, and manage multimodal health data with automation, audit trails, and APIs.

© 2026 Nimblemind. All rights reserved.