Virtusa Recognized as Global Leader in Gen AI Services by ISG Provider Lens® - Read report

solution

Accelerate life sciences content approvals with Virtusa’s compliant pre-MLR framework

Streamline medical, legal, and regulatory approvals for faster, error-free processes

Speak to an expert

Life sciences organizations often face slow, fragmented MLR (Medical, Legal, Regulatory) review processes. Disconnected teams, manual workflows, and inconsistent standards lead to delays, increase compliance risks, and hinder scalability — especially as global content demands continue to grow.

Traditional review models struggle to keep pace with the increasing volume of content across multiple markets and digital channels. Without centralized control, it becomes challenging to track version history, enforce governance, and maintain clear audit trails — all of which are critical for regulatory compliance and success.

Ensure that you open the links to enable the Next button, assuming you have read all the documents.
Okay & NextClick to Next

AI-driven pre-review intelligence

Virtusa’s advanced framework leverages AI to transform pre-MLR content checks. The solution pre-screens content for potential compliance risks, optimizes routing paths based on complexity and team availability, and reduces unnecessary manual intervention. This accelerates approvals while upholding the highest standards of regulatory rigor.

Virtusa pre-MLR framework

Specifically built for the life sciences industry, our pre-MLR solution combines structured processes, automation, and compliance oversight, seamlessly integrated into your existing content systems. Whether you use Veeva Vault, Adobe AEM, Salesforce, or a custom platform, Virtusa’s framework delivers faster approvals, fewer errors, and complete traceability.

Ensure that you open the links to enable the Next button, assuming you have read all the documents.
Okay & NextClick to Next

Key features

Virtusa’s compliant pre-MLR framework
  • Prebuilt workflow templates: FDA and EMA-aligned, customizable to fit your organization’s needs.
  • Integrated platform connectors: Easy integration with tools like Veeva Vault, Adobe, Salesforce, and more.
  • Role-based access and full audit trails: Secure stakeholder collaboration with mandatory compliance and auditability.
  • Automated version control: Maintain a complete history of content changes as required by regulatory guidelines.
  • Custom dashboards and real-time alerts: Inform stakeholders with live updates and performance metrics.
  • Multilingual and multi-brand support: Review and approve content globally, across regions and product lines.
Virtusa’s compliant pre-MLR framework

Key benefits

Enhance content approvals, minimize regulatory risks, and empower global teams with Virtusa’s Pre-MLR Framework, delivering measurable results where it matters most.

  • Up to 50% faster approval cycles: Powered by AI-accelerated workflows
  • Reduced regulatory risk: Enabled by standardized, auditable review processes
  • Increased productivity: For medical, legal, regulatory, and marketing teams alike
  • Centralized tracking and documentation: Covering all content operations in one place
  • Scalable support:  Ready to meet growing global content demands

VIDEO

Virtusa’s compliant pre-MLR framework 

Learn more about our offering

Speak to an expert

Ready to transform your MLR workflows?

Let Virtusa help you streamline approvals, ensure compliance, and accelerate your market readiness with confidence.

Ensure that you open the links to enable the Next button, assuming you have read all the documents.
Okay & NextClick to Next

Related content