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Knolens SLR

Fully automated Targeted and Systematic Literature Reviews (SLR)

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Knolens SLR: Automated, Accurate, and Audit-Ready Literature Reviews

An automated systematic literature review platform for pharma, biotech, and life sciences. Deployed across Boston, Cambridge, New Jersey, and global markets, it transforms manual review processes into AI-powered, audit-ready evidence generation.

Platform Definition
A flexible, high-accuracy AI solution for SLRs at pharmaceutical scale—supporting FDA submissions, regulatory filings, payer reimbursements, and new therapy evaluations worldwide.

Core Value Proposition
By extracting, synthesizing, and validating medical research, Knolens SLR delivers reliable, up-to-date evidence with full traceability and regulatory audit readiness—powering decisions across the drug development lifecycle.

What Makes Knolens SLR Stand Out

Flexible

Design your review, your way — from PICOS to regulatory-ready outputs.

  • Enter or upload PICOS criteria — even images — and customize extraction templates to match study or regulatory needs.
  • Easily add variables, adjust criteria, and configure workflows to align each SLR with clinical, regulatory, HEOR, or market access objectives.

Fast

  • Transform months of work into hours.
  • Complete abstract and full-text screening in under 30 minutes.
  • Extract and structure full data grids in less than 4 hours.
  • Minimize manual effort, maximize output, and accelerate evidence generation without compromising depth or compliance.

Accurate

  • Powered by Knolens’ trusted engine, SLR achieves 95%+ accuracy across over 500+ clinical, regulatory, and outcomes variables.
  • Each datapoint is fully traceable to its original source, ensuring audit-ready compliance for submissions, publications, and reviews.
  • Proprietary AI models, trained on domain-specific ontologies and workflows, deliver precision unmatched by general LLMs.

Industry Standard

  • Knolens SLR ensures full PRISMA compliance for transparent and reproducible literature reviews.
  • Instantly generate PRISMA flow diagrams, screening logs, audit trails, and complete source traceability.
  • Designed to meet regulatory, payer, and publication standards for scientific rigor and credibility.

Why Choose Knolens SLR?

Whether analyzing therapy landscapes, tracking disease progress, assessing biomarkers, or evaluating patient outcomes, it delivers the depth and accuracy needed to drive life sciences forward.

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Book a free demo to see how Knolens SLR automates literature reviews for regulatory, market access, clinical, and competitive needs—helping pharma teams worldwide optimize evidence synthesis workflows.

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