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 and the TMF 101 - Blog 1: Basics of a Clinical Trial

Introduction  Firstly, welcome, it is great to see you here. Thank you for taking the time to check out our new blog series on the basics of Clinical Trials and the TMF. This series is designed to be

FDA and MHRA Say Remote and Hybrid Inspections to Continue

At the 2022 Drug Information Association Annual Meeting, held in-person in Chicago June 20-23, representatives from the compliance offices of the FDA and MHRA gave a detailed assessment of the pros

Examining the Why and How of Integrating Your eTMF and CTMS

Adapted from a Phlexglobal Ask An Expert interactive discussion held May 11, 2022 and available on-demand here.   Why Integrate Your CTMS and eTMF Systems?  A typical electronic Trial Master File

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It's time to raise your standard 

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