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Document Processing in Pharmaceuticals

Pharmaceutical companies process enormous volumes of documents across every stage of a drug's lifecycle — batch manufacturing records, certificates of analysis, clinical study reports, regulatory submission dossiers, adverse event case reports, and supplier qualification packages.

Slow or inaccurate document processing delays product releases and regulatory approvals, creating compliance exposure that threatens revenue and market position.

LandingAI transforms documents into highly accurate, verifiable, structured data so teams can reliably automate document-intensive workflows.

Why Agentic Document Extraction for
Pharmaceuticals

Faster Regulatory Submission Cycles

Extracting and structuring data from clinical study reports, CMC dossiers, and supporting technical documents accurately on the first pass compresses submission timelines and reduces the back-and-forth with review teams that extends approval windows.

Faster Regulatory Submission Cycles

Audit-Ready Traceability by Default

Every extracted value is grounded to its precise location in the source document, giving quality and compliance teams a defensible, complete record across batch records, deviation reports, and regulatory filings without any additional annotation effort.

Audit-Ready Traceability by Default

Scale Without Proportional Headcount

Pharmaceutical document volumes grow continuously across development programs, product lines, and markets — agentic extraction allows quality, regulatory, and pharmacovigilance teams to absorb that growth without proportional increases in manual review staff.

Scale Without Proportional Headcount
Key capabilities

Built for Complex Pharmaceutical Documents

Intelligent document processing across branded drug development, generic manufacturing, specialty pharma, and over-the-counter production is extremely difficult due to the sheer diversity of document types, the inconsistent layouts and the domain expertise required. Then add multiple languages, handwriting, photographs, scans and faxes to the complexity.

Accurate parsing of dense tables that span multiple pages and contain merged cells.

Single pipeline for image, slide, document, and spreadsheet file types with 1000+ pages.

Strong recognition of character-based languages, handwriting, checkboxes, stamps and signatures.

Schema-driven field extraction with visual grounding traceable to the original document.

Use cases

Regulatory Submissions

Regulatory Submissions

Extract and structure data from Common Technical Document modules, clinical study reports, investigator brochures, nonclinical study summaries, and CMC dossiers to assemble complete, accurate regulatory packages.

Impact
  • Accelerate submission readiness and reduce time from data lock to dossier completion
  • Cut manual authoring and compilation effort across regulatory affairs teams
  • Eliminate extraction errors that trigger agency queries and extend review timelines
Batch Record Review

Batch Record Review

Automate extraction of manufacturing parameters, in-process control results, and analytical test data from executed batch records, deviation reports, and laboratory notebooks to support batch release decisions.

Impact
  • Compress batch release cycles and bring product to market faster
  • Reduce QA reviewer time spent on manual data transcription and cross-referencing
  • Flag discrepancies between specification limits and recorded results before they become audit findings
Pharmacovigilance Case Processing

Pharmacovigilance Case Processing

Extract patient, product, and adverse event data from individual case safety reports, medical literature, and spontaneous reports to support signal detection and aggregate safety reporting obligations.

Impact
  • Protect market authorization by meeting mandatory safety reporting deadlines consistently
  • Reduce case processing cost per ICSR through automated data extraction and coding
  • Improve signal detection accuracy by ensuring complete, consistently structured case data

Trusted for Document-Heavy Pharmaceutical Workflows

Agentic Document Extraction enables pharmaceutical companies to automate document-intensive processes that traditionally require manual review.

Agentic Document Extraction has proven to be both accurate and easy to use. We are building on that foundation to deliver reliable, transparent, and scalable automation that our customers can validate and trust.”

View case study →
Business Process Automation
Neil Walker
Neil WalkerHead of Product, TCG Process
TCG Process

ADE has significantly outperformed other document extractors we’ve used. It has helped us build an Agentic RAG answer engine, based on unique healthcare institutional content, to offer instant, validated support to medical professionals at the point of care.”

View case study →
Fortune 100 Financial Services
Head of Data & Analytics, Global Financial Services Firm

Trust is the product. Accuracy alone isn’t enough at enterprise scale—what matters is provenance, traceability, and control. LandingAI gives us confidence that every extracted value can be traced back to its source, audited, and defended. That’s what makes it deployable in regulated, real-world environments.”

View case study →
HealthTech Platform
Dr. Declan Kelly
Dr. Declan KellyFounder and CEO, Eolas Medical
Eolas Medical

Agentic Document Extraction has proven to be both accurate and easy to use. We are building on that foundation to deliver reliable, transparent, and scalable automation that our customers can validate and trust.”

View case study →
Business Process Automation
Neil Walker
Neil WalkerHead of Product, TCG Process
TCG Process

ADE has significantly outperformed other document extractors we’ve used. It has helped us build an Agentic RAG answer engine, based on unique healthcare institutional content, to offer instant, validated support to medical professionals at the point of care.”

View case study →
Fortune 100 Financial Services
Head of Data & Analytics, Global Financial Services Firm

Trust is the product. Accuracy alone isn’t enough at enterprise scale—what matters is provenance, traceability, and control. LandingAI gives us confidence that every extracted value can be traced back to its source, audited, and defended. That’s what makes it deployable in regulated, real-world environments.”

View case study →
HealthTech Platform
Dr. Declan Kelly
Dr. Declan KellyFounder and CEO, Eolas Medical
Eolas Medical

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Production-ready AI extraction pipeline with document understanding built for production.