INDUSTRY

Pharma & Medical Devices

Run regulated operations with confidence. Standardize contracting, support global compliance, and maintain full audit trails.

10x faster contract processing

10+ YEARS SERVING GLOBAL ENTERPRISES

Leah for Pharma & Medical Devices

Pharmaceutical and medical devices organizations face intense regulatory demands, massive contract volumes, and global operational complexity.

Leah streamlines contracting, ensures compliance, and delivers real-time intelligence purpose-built for regulated environments.

Quicken Contracts

Accelerate contract creation and workflows—reducing cycle times and improving efficiencies across your contracts.

Improve Visibility

Surface critical terms, obligations, and exposure points across contracts and suppliers to make faster, more confident decisions.

Ensure Compliance

Maintain control with audit-ready documentation, traceable updates, and built-in support for regulated environments.

“We reduced contract migration effort by 70% through AI-powered extraction, unified contract management for 1,300+ global users, and improved response times across the platform.”

-  Global Pharmaceuticals Company

See What Leah Can Do For You

A group of healthcare professionals reviewing test results

Accelerate contract workflows with AI precision.

Use AI-powered drafting, templates, and clause libraries to generate high-volume contracts like R&D and non-disclosure agreements.

Automate pre-approved workflows and playbooks by contract types, value thresholds, teams, and regions to eliminate manual tracking and follow-up.

Access instant policy and regulatory insight with conversational AI that guides teams on standards, negotiation strategy, and compliance requirements.

A surgeon looking at a small vial

Unlock deeper visibility across every contract and supplier.

Customize reports and dashboards that display important contract information to provide executives with visibility into contractual data.

Gain greater insight into R&D partnerships and non-disclosure agreements, and increase control over all contract-related data.

Easily retrieve delivery obligations in supplier contracts and assign tasks to business owners to ensure deliverables are completed and tracked effectively.

A woman preparing a slide for a microscope

Stay ahead of regulatory compliance requirements.

Maintain audit-ready documentation with full traceability, automated extraction, and structured compliance records.

Instantly surface regulatory requirements in contracts and ensure alignment with GxP, 21 CFR Part 11, and other global standards.

Query your contract portfolio via conversational search to identify and manage deviations and high-risk clauses.

Why Leah?

  • Pharmaceutical Expertise
    Trained on pharmaceutical contract language, Leah delivers regulatory-grade precision by automatically extracting data from quality agreements, clinical trial contracts, and licensing terms.
  • Compliance StrengthLeah delivers regulatory compliance with 21 CFR Part 11 compliance for e-records and signatures, audit trail transparency, formal validation processes, and support for GxP and multi-jurisdictional reporting.
  • Integration EcosystemNative integration with SAP/Ariba, DocuSign, and specialized solutions for quality management and clinical operations ensures frictionless alignment with your pharmaceutical tech stack.

Ready to take your operations to the next level?