AI-Driven Contract Intelligence for Regulated, Research-Driven Environments

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​Health and Life Sciences organizations manage highly complex and regulated contracts across clinical trials, research collaborations, supplier sourcing, and quality compliance.
NexvisionIX CLM/CPM delivers a unified platform to streamline contract creation, ensure regulatory alignment, and monitor performance—powered by intelligent automation and AI agents.
Empowering life sciences companies to accelerate revenue, reduce risk, and enforce quality through intelligent contracting and digital transformation

What Makes Health & Life Sciences Contracts Unique?

Highly Regulated Environments

Life sciences contracts must comply with standards like 21 CFR Part 11, HIPAA, and GxP, requiring audit trails, digital signature validation, and regulatory reporting features to ensure full legal defensibility.

Frequent Amendments During Trials

Trials evolve rapidly, resulting in ongoing amendments. Effective management of these changes requires dynamic workflows, clause tracking, and version control to avoid regulatory and contractual risks.

Multi-Party, Multi-Jurisdictional Complexity

These agreements involve cross-border collaboration with pharma, CROs, universities, and regulators, requiring legal harmonization and local jurisdiction awareness for data sharing and ethics compliance.

Volume-Heavy Workflows

From CDAs and CTAs to MSAs and Supply Agreements, organizations manage hundreds of contracts, each with timelines, stakeholders, obligations, and auto-renewal risks that require AI-driven oversight.

Our platform combines life sciences expertise with enterprise-grade AI to streamline the full contract lifecycle — from drafting to compliance.

AI Agents Purpose-Built for Life Sciences Contracting

NexvisionIX deploys a suite of AI agents that augment every stage of the contract lifecycle—from authoring to performance tracking—tailored for health and life sciences use cases.

Obligation Intelligence Agent

Extract and monitor regulatory and clinical trial obligations from contracts.

Clinical Trial Performance Agent

Monitor CRO or site performance against trial milestones and SLAs.

Supplier/Vendor Risk Agent

Track GMP vendor compliance, quality scores, delivery timelines, and audit triggers.

Revenue & Pricing Compliance Agent

Monitor pricing agreements, chargebacks, rebates, and anti-kickback compliance.

Regulatory & Quality Audit Agent

Ensure contracts align with evolving FDA, EMA, and ISO quality standards.

Smart Renewal Agent

Flags underperforming partnerships or contracts needing renegotiation.

These AI agents operate collaboratively and contextually, adapting to contract type, business function, and compliance scope.

End-to-End Use Cases for CLM + CPM

Confidential Disclosure Agreements (CDAs)

AI-assisted clause drafting, version control, and auto-expiry triggers.

Clinical Trial Agreements (CTAs)

Fallback language, jurisdiction-specific logic, and trial-milestone tracking.

Supplier Contracts

SLA-based vendor evaluation, quality tracking, and risk-based renewal insights.

Manufacturing Contracts

One-click pricing amendments, batch release schedules, and fulfillment tracking.

Quality & Compliance Agreements

CFR Part 11-compliant signature flows, GxP audit logs, validation history.

Performance Monitoring

Role-based dashboards for R&D, compliance, procurement, and legal teams.

Built-In Intelligence Across the Contract Lifecycle

Accelerated Revenue

Automates rebates, chargebacks & tiered pricing.
Links sales/outcomes to contract terms across GPOs, PBMs, and HCPs.

Supplier & CDMO Insights

Monitors timelines, yields, quality, and obligations.
Flags delays or risks in clinical supply and manufacturing.

Multiparty Contracting

Manages complex agreements across CDMOs, CROs, 3PLs, and care networks.
Enables full performance oversight.

Regulatory Alignment

Enforces FDA, EMA, GMP, 340B & pricing rules.
Auto-generates audit trails and supports QA/legal teams.

AI-Powered Optimization

Scores vendor risk, tracks SLAs, and reduces overhead.
Integrates with Veeva, SAP, Medidata, and more.

Key Capabilities

AI-Powered Authoring

Clause recommendations and fallback options based on contract type and region.

Regulatory Compliance Automation

Built-in validations for FDA, EMA, HIPAA, and GxP requirements.

Self-Service Templates

Enable teams to initiate compliant contracts with legal-approved structure and oversight.

Mass Amendments Engine

Apply scope, pricing, or regulatory changes to hundreds of contracts at once.

Real-Time Dashboards

Track SLAs, site activations, renewal risks, and financial exposure in real time.

End-to-End Integration

Connects with CTMS, eTMF, LIMS, ERP, and sourcing platforms for seamless flow.

Built for Tomorrow’s Life Sciences Ecosystem

• GxP & HIPAA-ready workflows
• Clause libraries customized for research, trials, and suppliers
• Pre-validated integrations with ERP, LIMS, CTMS
• Continuous AI learning from historical contract behavior
• Interactive dashboards and performance alerts

Explore the Future of Intelligent CLM & CPM

Book a demo today to see how NexvisionIX’s Health & Life Sciences vertical can help you:
Accelerate trial onboarding · Stay compliant with global regulations · Monitor supplier and clinical performance · Adapt quickly to regulatory and scientific changes

Book a Demo