PHARMA &
LIFE SCIENCES AI
REGULATORY-READY AI DATA
Accelerate AI-driven drug and device development using GxP-aligned annotation, audit-ready workflows, and clinical-expert validation.
EXPERIENCED LEADER
IN CLINICAL AI
iMerit supports clinical outcomes and pharmacovigilance models across oncology, gastroenterology, dermatology, radiation oncology, and more; delivering domain-specific data services that accelerate AI development in critical clinical settings.
WHY CHOOSE iMERIT
FOR YOUR DIGITAL CRO
iMerit delivers expert-led clinical data annotation and scalable, secure infrastructure to accelerate AI development across diverse medical domains. With GxP-ready workflows, regulatory compliance, and a global team of certified clinical professionals, we ensure high-quality, audit-ready data for clinical and pharmacovigilance AI.
EXPERT-LED
CLINICAL ANNOTATION
Our workforce includes onshore and global board-certified experts and clinical coders; ensuring precision and domain expertise across clinical trials and real-world datasets through expert annotation services.
GxP-READY
WORKFLOWS
Built-in audit trails, structured metadata, and 21 CFR Part 11-compliant processes provide full traceability and regulatory confidence across all data labeling workflows.
SCALABLE & SECURE
INFRASTRUCTURE
Our global delivery framework includes dual-shore, offshore, and tiered workforce models, optimized for cost, quality, and speed. We’re fully compliant with HIPAA, ISO 27001, SOC 2, and support on-prem, hybrid, and cloud-based deployments.
iMerit serves as a strategic partner in building regulatory-compliant, clinically validated datasets—reducing risk, cutting development time, and boosting AI model performance for life sciences and pharmaceutical companies.
HOW IT WORKS
iMerit provides end-to-end, regulatory-grade clinical data annotation services that accelerate AI development while ensuring precision, compliance, and scalability.
- CONSULTATION & DESIGN WORKFLOWS
Analysis of complex visual scenes for object detection, segmentation, classification and tracking. - DATA ANNOTATION & QUALITY CONTROL
Our clinical experts execute precision annotation workflows using custom SOPs, embedded QC checkpoints, and automated audit trails. - DELIVER & VALIDATE
We deliver validated, labeled datasets with performance benchmarks designed for FDA/EMA submissions and real-world model testing. - SCALE & EXTEND
With secure, scalable operations, we help teams rapidly expand to new trial sites, therapeutic areas, or modalities.
USE CASES
Delivering domain-aligned use cases across research, clinical trials, safety, and compliance.
Clinical Trial Data Annotation
Transform multimodal trial data into structured, high-quality datasets for AI model training, monitoring, and regulatory submissions.
Medical Imaging for Drug Development
Annotate MRI, CT, X-ray, and pathology images to identify biomarkers, track disease progression, and assess treatment response.
Regulatory-Ready Dataset Preparation
Curate validated datasets with full traceability to meet FDA/EMA submission requirements.
Drug Discovery Data Labeling
Annotate molecular structures, assay outputs, and chemical interactions for AI-powered compound screening and optimization.
Fortune 500 Medical Device Company
Trusted & secure
At iMerit, data security and privacy are built into every workflow. Our platform features strict access controls, granular data partitioning, and encryption for sensitive information, and complies with data privacy regulations and compliance standards. Detailed logging, monitoring, and audit trails ensure complete transparency and traceability, keeping every interaction with your data secure and accountable.
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The need for speed in high-quality data annotation has never been greater. iMerit combines the best of predictive and automated annotation technology with world-class data annotation and subject matter experts to deliver the data you need.
