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Create Perfectly Formed PDFs

Submissions-ready PDF content is essential to ensuring quick and confident review by regulatory bodies. Adlib is 15+ year leader in this space, helping to ensure our customers get the ideal output:

  • searchable
  • hyperlinked
  • bookmarked
  • ISO validated
  • stamped with fully enriched metadata

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Created Perfectly Formed PDFs

Help Communities Faster

For Life Sciences, patents expire quickly so the millions of dollars, hours and documents involved in bringing drugs and devices to communities that need them must be optimized and accurate. Adlib can help.

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Help Communities Faster
Time to ROI

Make Regulatory Review Seamless

Agencies like the FDA demand flawless, submissions-ready PDF content to ensure quick and confident review and approval. Adlib solutions expedite your time to market with impeccable automation.

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Make Regulatory Review Seamless


Customer Success Stories

Learn how Adlib helps organizations around the world to bring automation and AI to critical workflows.

Getting life-saving products to market sooner

Aldib IconChallenge

FDA and other global regulators demand high-quality electronic submissions to approve new drugs and devices from Life Sciences leaders. Creating perfect PDF submission content manually was slow, inconsistent and expensive – delaying approvals and reducing time in market under patent.

Aldib Orange IconSolution

Adlib delivers industry leading and fully automated PDF transformation and enhancement capabilities reducing costs, improving quality and ensuring consistency for submissions content enabling regulators to easily navigate and approve submissions.

See how we can help with your critical workflows.

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