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Pharma, Biotech & CRO Companies Trust Adlib to:

  • Automate Clinical Trial Processes

  • Generate Regulatory-Compliant Submissions

  • Create Audit-Ready Documents of Record

  • Streamline M&A Documentation


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Delivering a Critical Vaccine: How Document Conversion Saved the Day

The clock was ticking for a top pharmaceutical company’s vaccine team. After a year of a compressed vaccine development timeline for a life-saving vaccine that held the key to solving a global public health crisis, the Global Vice President of Vaccines at a top pharmaceutical company came to Adlib in a panic.

With hours to go before the final step on their emergency authorization application for the U.S. Food & Drug Administration (FDA), the system crashed. And crashed again. The entire approval submission was in jeopardy.

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Transform dark and unstructured data into regulatory compliant documents.

Technically Compliant TMF and eCTD

Avoid documentation errors, simplify submission processes, and decrease rejection rates.

Audit-Ready Investigator Site Files (ISFs)

Reduce the time and effort needed to maintain ISF files and prepare them for inspection.

Compliant M&A Documentation

Streamline documentation throughout deal lifecycles and ensure regulatory compliance.


Automate error-prone, time-consuming, manual documentation processes.

Increase Operational Productivity

Automate tasks and reduce manual efforts needed to manage TMF and eCTD documentation.

Boost Internal Connectivity

Create standardized documents to improve data sharing throughout the enterprise.

Streamline Quality Control

Improve quality planning, quality control, and quality assurance documentation processes.


Reliable integration with eTMF, RIM, QLM and other software systems.

Create a Document Repository

Assemble and maintain critical data within a centralized and accessible document repository.

Eliminate System Silos

Reduce IT budgets and technology footprints via integration with existing tech-stacks.

Leverage Critical Data

Standardize unstructured files to create searchable, analytics-ready documents.

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“It is now much easier to monitor documents volumes, accuracy, and standardization with Adlib,”

- Systems Engineer, A Leading Global Pharmaceutical Company

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How Adlib Helps
Life Sciences Companies


and ingest trial and regulatory documentation from any source.


from unsearchable formats into machine-readable and FDA-compliant PDFs.


and assemble multiple files into cohesive / digitally-tagged documents. 


documentation by adding headers, footers, watermarks, and tables of contents.


and save files into user-specified folders for downstream processing.


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Adlib Wants To Help!

Book a meeting with a Digital Transformation Expert, and let’s see if Adlib can help you work better, faster and smarter and help you stop wasting time, money and effort.

If we can help, we can usually help in a BIG way.
If we can’t help, we’ll let you know that too! 

Featured Resources

LS ebook Speed to market web

Unlocking Speed To Market: Working Smarter, Moving Faster in Life Sciences

LS Guide - One-pill solution web
Industry Guide

Overcoming Challenges in Clinical & Regulatory Operations With AI

Adlib Whitepaper - Best Practices For Effective Document Archival Cover web

Best Practices For Effective Document Archival

Finer POints of Document Security Social

The Final Points of Document Security