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Enabling Life Sciences Companies to Meet Compliance Mandates & Enhance Vital Business Processes

Adlib PDF is used by 90% of the top 100 Life Sciences companies to improve the efficiency of document lifecycle workflows. Why?

As the leading rules-based, compliant document transformation platform for Life Sciences, Adlib PDF integrates with Enterprise Content Management (ECM) systems, Product Lifecycle Management (PLM) and other business applications to support critical document processes. Adlib PDF is THE trusted Advanced Rendering technology in the Life Sciences space.

Integrating with Enterprise Content Management (ECM) Systems

Integrating with key business tools, including all leading Enterprise Content Management (ECM) systems, Adlib PDF is driven by the most powerful, automated document-to-PDF conversion engine in the market.

Ideal for:

  • Life Sciences organizations—including pharmaceutical, biotechnology and medical device companies—seeking metadata-driven, intelligent and compliant document-to-PDF document transformation solutions that can scale from single departments to shared services across an entire organization.
  • Systems Integrators that need to deliver unparalleled solutions to increase efficiencies in the regulatory approval process, streamline workflows and scale massively to support enterprise environments. Systems Integrators interested in partnering with Adlib should join the Adlib Partner Plus program.

Datasheet: Adlib PDF for Life Sciences

Advanced Rendering technology provides an intelligent and compliant document-to-PDF process, creating streamlined efficiency for document workflows for organizations in the Life Sciences arena.

Best Practices

  • Intelligently apply metadata-based enhancements, like headers, footers, watermarks, digital signatures and security settings.
  • Ensure content is accessible regardless of viewing platform by publishing to PDF/A, the ISO standard for archiving
  • Automatically and accurately render documents in their native language, ensuring content is in compliance with global regulatory requirements.

Solutions

  • Garner efficiencies in the regulatory approval process and streamline workflows with regulatory requirements set out by FDA & other health agencies
  • Increase accuracy and reduce risks of human error associated with manual processes by automatically transforming documents with Advanced Rendering capabilities
  • Scale massively to support the enterprise with Adlib’s centralized solution that maintains high availability, load balancing and full reporting in support of high-volume, multi-site environments, including those that process millions of documents per day
Achieving Cost Savings and Compliance in Life Sciences Manufacturing
Achieving Cost Savings and Compliance in Life Sciences Manufacturing
Achieving Cost Savings and Compliance in Life Sciences Manufacturing
Find out how a multinational consumer pharmaceutical organization reduced manufacturing downtime and achieved regulatory compliance with Adlib.
Reducing Costs through Better Practices
Reducing Costs through Better Practices
Reducing Costs through Better Practices
Hear how a designer and manufacturer of respiratory care products reduced costs and improved efficiencies with Adlib’s server-based solution.
Unifying Platforms for Improved Efficiencies with FDA Submissions
Unifying Platforms for Improved Efficiencies with FDA Submissions
Unifying Platforms for Improved Efficiencies with FDA Submissions
Explore how a global pharmaceutical organization integrated a diverse range of publishing systems into a single environment with Adlib, resulting in millions of dollars in cost savings.