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Medical Legal Review

Streamline. Comply. Accelerate.

Acheron's Medical Legal Review (MLR) solution provides a comprehensive platform to manage MLR reviews and approvals, ensure regulatory compliance, and accelerate the end-to-end marketing production process for Life Sciences companies.

Transforming MLR for Life Sciences

Medical Legal Review (MLR) has always been one of the most challenging and complex aspects of the marketing production process for Life Sciences companies. Organizations need a fresh approach to MLR that enables a timely and efficient marketing workflow and allows for rapid process innovation.

Acheron's MLR solution, built on OpenText Media Management and AppWorks platform, replaces manual processes with system-driven workflows and lifecycles, enabling upstream creation, promotional/regulatory review, and downstream publishing/distribution in one unified system.

Key Features & Capabilities

1. Comprehensive MLR Workflow Management

End-to-end lifecycle management of promotional materials with system-driven workflows

  • Single source for Planning, Tracking, Authoring and Publishing regulated content
  • Configurable workflows aligning to various market needs
  • Workflow and Audit tracking mechanisms with notification capabilities
  • Reference and Relationship management linking global contents

Outcome: Streamlined MLR processes with complete visibility and control

2. OpenText Integration & Content Management

Built on OpenText Media Management and AppWorks platform for robust content operations

  • Leverages OTMM for content management, versions management, metadata, and search
  • AppWorks integration for lifecycle management and external system integration
  • Unified experience combining Media Management and workflow operations
  • Fully integrated with various upstream and downstream channels

Outcome: Seamless content operations with enterprise-grade media management

3. Regulatory Compliance & Security

Enhanced compliance features with CFR Part 11 support and audit capabilities

  • CFR Part 11 compliance for regulated environments
  • Auto FDA Form Generation for streamlined submissions
  • Secured access and structural storage of content across the globe
  • Enhanced audit and history views with timeline tracking

Outcome: Stronger regulatory compliance with reduced risk and faster approvals

4. Advanced Collaboration & Analytics

Enhanced collaboration tools with comprehensive analytics and reporting

  • Digital collaboration with asset annotations and review comments
  • MLR Analytics for performance insights and optimization
  • Multiple work buckets view for efficient task management
  • Task delegation and pull task capabilities

Outcome: Improved team productivity and data-driven decision making

Product Highlights

Stronger Regulatory Compliance

Enhanced compliance features with CFR Part 11 support and comprehensive audit trails

Reduced Time to Market

Accelerated approval processes with automated workflows and improved global brand consistency

Multi-channel Publishing

Point & Click distribution and automated withdrawal across multiple channels

Improved Efficiency

Enhanced team productivity through stronger collaboration across internal and external agencies

MLR Release 16.5 Highlights

Latest version of MLR solution is fully supported for OpenText 16.5 with enhanced features and capabilities

Enhancement in inside-out OTMM UI experience
Ability to submit 'Reference Only' assets
Submission with parent child relationship
(Re)Submit an existing asset from Media Library (OTMM)
Flexible and Configurable workflows per Region
Advanced search and pagination support
Ability to add additional approvers without modifying workflow
Enhanced Metadata view and Reference relationship view
Timeline view with expected and actual timelines
iSales App (Simplified Approved Assets App for Sales team)

Who We Help

Life Sciences Companies

Pharmaceutical and biotech companies managing promotional material reviews and regulatory compliance

Marketing & Creative Teams

Teams responsible for creating and managing promotional content requiring MLR approval

Regulatory Affairs

Regulatory professionals ensuring compliance with FDA and global regulatory requirements

IT & Operations

IT teams seeking to digitize and streamline MLR processes with enterprise-grade solutions

Key Integrations

Built on OpenText platform with seamless integration across the enterprise ecosystem

OpenText Creative Review
OpenText Analytics
OpenText AppWorks
OpenText OTMM

Transform Your MLR Process Today

Ready to digitize, streamline, and accelerate your Medical Legal Review process? Let Acheron help you implement a comprehensive MLR solution that ensures compliance while improving efficiency.

Comprehensive workflow management
Enhanced regulatory compliance
Reduced time to market
Improved team productivity

Unlock Your Enterprise's Full Potential Today

Ready to streamline your operations, accelerate innovation, and achieve unparalleled efficiency? Partner with Acheron.