Phlexglobal Regulatory Software

Our product offerings are considered highly innovative in the industry for their out-of-the-box best practices capabilities, use of automation technology, and user-focused design.


Why Choose Phlexglobal Regulatory Software?


Faster time to approval


Optimized revenue opportunities


Increased efficiency and accuracy

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Improved planning and tracking of regulatory activities


Faster, more accurate Health Authority communications

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Global compliance with current and future needs



Registration planning, tracking and management built for both your data and automation of your key processes.

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A single regulatory database that will help you to avoid redundant data that exists within your submissions.

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Control all your documents in one place. Share it with your colleagues in a controlled environment.

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Comprehensive xEVMPD software for managing your medicinal product information.

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A complete submission publishing solution for life sciences.

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Out-of-the-box, pre-configured & validated eCTD solution.

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Latest News

Entering the Post-Paper Realism: The Principles of Cyber Ethics

The Shoulds and Shouldn’ts of Electronic Systems and Data in Clinical Trials Intro With the word should being mentioned 569 times and constituting ~7% of the content (only outweighed by data – 618

Overcoming TMF misfiles and metadata errors to reduce inspection risk

Trial master file misfiles are a common occurrence, with as many as one in every 10 documents being misfiled.   In some ways, misfiles are an even greater issue now with eTMF systems, where filing is

TMF Management in Clinical Trials Blog 3: Running the Trial in Your eTMF

Introduction Well, first and foremost, welcome!   Rob Jones has relinquished control and I’ve been given free rein to bring you the last blog in the series on TMF Management in Clinical Trials. Those

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