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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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

Clinical Trials & the TMF 101 - Blog 4: The TMF Trinity

Introduction We have been on a journey you and me, we started off by understanding the purpose of a clinical trial and the multiple phases to get products to market. We then looked at the Trial

Clinical Trials & the TMF 101 - Blog 3: Paper vs Electronic, why it is more than a DMS

Introduction Awww it warms my heart you came back to read the third blog. I hope you are finding these helpful, don’t forget to send any of your feedback or questions to We

Clinical Trials & the TMF 101 - Blog 2: What is this TMF you speak of?

Introduction You came back, great! I hope you enjoyed our first blog in this series which was all about the basics of a clinical trial. In this blog we are going to get into the Trial Master File,

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