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Built for Pharma:
Simplify Compliance.
Accelerate Clinical Operations. Protect Data Integrity.

Manage SDEAs and regulatory contracts in one secure CLM, built for GxP, FDA, and EMA compliance, and designed to accelerate execution across every stage of pharmaceutical operations.

User communicating with Dilitrust AI

Operational Complexity is Quietly Eroding Compliance

Regulatory
Overload

20+ global authorities, including the FDA, EMA, ANVISA, MHRA, and others, issue ongoing updates that make manual SDEA oversight nearly impossible.

Data
Fragmentation

Contract data is spread across emails, shared drives, and spreadsheets, leading to limited visibility and inconsistent documentation.

Compliance
Risk

Lack of automation causes version errors, missed renewals, and audit findings that expose teams to compliance penalties.

Legal teams spend up to 40% of their time on administrative work instead of high-value legal or clinical activities.

Ensure Compliance
Without Slowing Operations

Automate regulatory workflows and approvals across your organization. Reduce manual effort and stay aligned with GxP, FDA, and EMA standards.

Gain 360° Visibility
on Your Contracts & Data

Monitor every agreement, obligation, and SDEA in real time. Centralize insights to eliminate silos and ensure traceability.

Protect Sensitive Data
with Confidence

Safeguard intellectual property and patient information. Meet GDPR and HIPAA requirements with built-in data security.

Measurable Efficiency. Proven Compliance.

33% faster
contract cycle time

Faster renewals and regulatory updates

9% average
cost savings

Through automated contract workflows

Up to 9.2%
revenue loss avoided

By eliminating poor contract management

100% audit trail
traceability

Ensured by DiliTrust’s GxP-compliant CLM

Trusted by Pharma Leaders Worldwide

Explore How Our CLM Works in Practice for Pharma

See how our CLM module helps you improve operational excellence, ensure compliance, and deliver measurable ROI.

Simple

Contract Management Made Easy

  • Store and manage a vast array of contracts specific to the pharmaceutical industry 
  • Enjoy unlimited storage for all your contract documents, ensuring easy access and retrieval 
  • Simplify contract negotiation processes, saving time and resources 
  • Reduce contract cycle time, enabling faster decision-making and agility in operations 
  • Leverage AI technology to quickly analyze and extract insights from contracts in various languages 
  • Foster collaboration among cross-functional teams, enhancing productivity and efficiency 
Flexible

More Flexibility, Enhanced Efficiency

  • Personalize your CLM platform to comply with the ever-changing regulatory context of the pharmaceutical industry, thanks to custom objects and workflows 
  • Identify opportunities to improve contract performance through 
    data-driven and pharmaceutical-specific KPIs and insights
  • Accommodate a wide range of contract types, including clinical trial agreements, manufacturing contracts, and distribution agreements 
  • Enable real-time collaboration and tracking during the negotiation and execution phase to mitigate risk and close deals faster
  • Integrate with existing systems and platforms, ensuring interoperability and data consistency 
  • Align contract management practices with organizational values and objectives, fostering a culture of corporate governance and ethics 
Reliable

Creating Trust Through Reliability

  • Ensure compliance with industry regulations and standards, including GxP and FDA/EMA requirements 
  • Benefit from a single source of truth for all your pharmaceutical contract data, ensuring information integrity and reliability 
  • Leverage robust approval workflows and electronic signature capabilities, enabling seamless contract execution and management 
  • Protect sensitive intellectual property and patient data with advanced security features and encryption protocols 
  • Maintain compliance with data privacy regulations such as GDPR and HIPAA, safeguarding sensitive information 
  • Access comprehensive audit trails of all contract activities, providing transparency and accountability 
  • Ensure compliance contractual obligations while minimizing risk are minimized, fostering trust and confidence among stakeholders

How To Properly Set Up Your CLM To Better Manage SDEAs

Streamline Contract Management in Highly-Regulated Industries

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Global Reach

Deployed in 64+ countries with local support on 3 continents.

Scalable by Design

From local affiliates to global compliance teams: one platform for all.

Certified Security

ISO 27001, ISO 27701, SOC 2, GDPR, and HIPAA compliance built in.

Insights by Role

Tailored content to help every stakeholder in Pharma
improve compliance, collaboration, and operational efficiency.

Simplify complex regulatory contracts across global markets.

Centralize SDEAs, supplier, and R&D agreements in one CLM to ensure full compliance with GxP, FDA, and EMA standards.

Compliance
& Quality Director

Automate clause tracking, approval workflows, and documentation to align with ALCOA, GDPR, and HIPAA requirements.

Clinical Operations & Pharmacovigilance

Accelerate collaboration while reducing compliance risks.

Ensure real-time visibility on all safety data exchange agreements and automate updates as regulations evolve.

Procurement
& Supply Chain

Secure supplier contracts with full traceability and oversight.

Monitor obligations, renewals, and performance in one repository — ensuring data integrity and regulatory continuity.

From Complexity to Compliance.
From Risk to Reliability.

Discover how DiliTrust helps pharmaceutical companies simplify compliance, streamline operations, and protect sensitive data, without sacrificing speed or visibility.

Automated Compliance Workflows

Streamline approvals, renewals, and audit preparation: stay inspection-ready 24/7 across all sites.

Real-Time Data Integrity

Monitor contractual obligations and regulatory milestones in one place. Eliminate data silos and Excel chaos.

Audit-Ready from Day One

Meet FDA, EMA, GxP, and GDPR standards effortlessly, compliance built by design, not by exception.