Don’t Let Your Documents Slow You Down.

The 300-plus days it takes for a regulatory agency to approve a new drug application can seem like a lifetime for a patient who is waiting for your new therapeutic.

We support thousands of regulatory and clinical operations specialists, helping them satisfy the complex demands of clients and regulators.



  • Tables of Contents
  • Appendices
  • Figures
  • Tables
  • Cross-references


Find and Fix:

  • Styles and format
  • Abbreviations
  • Phrases
  • Symbols
  • Formats



  • eCTD/ICH format
  • Completeness
  • PDF readiness

You Need to Take the Fastest Path to Compliance.

Be certain your eCTD will meet your company’s and regulatory agencies’ review standards with DocXtools™ for Life Sciences.

Did you know?

88% of medical writing professionals believe they could complete submissions faster by using technology.
Litera Microsystems Market Research (2017)

Transform your documents.

Create and review documents faster.

Format documents and find/fix deviations from your standards in record time.

Empower your authors and review teams.

Produce high-quality submissions efficiently.

Mitigate risk.

Let the software focus on document integrity so you can focus on the contents.

Get help when you need it.

Our help desk provides ongoing support and expert assistance when you need it most.

As a direct result of implementing DocXtools for Life Sciences, we have eliminated reiterative manual checks of our documents, freeing up our staff to take on more projects.
Cullen Vogelson, President, Illuminated Research
DocXtools for Life Sciences saves time. It gives you a quicker way to go through the abbreviations in your document, so you can set that task aside and devote your time to the more important content.
Senior Medical Writer, Global Pharmaceutical Company