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.

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Why Choose Phlexglobal Regulatory Software?

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Faster time to approval

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Optimized revenue opportunities

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Increased efficiency and accuracy

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Improved planning and tracking of regulatory activities

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Faster, more accurate Health Authority communications

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Global compliance with current and future needs

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PHLEXRIM

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

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PHLEXIDMP

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

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PHLEXEVMPD

Comprehensive xEVMPD software for managing your medicinal product information.

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PHLEXSUBMISSION

A complete submission publishing solution for life sciences.

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PHLEXSUBMISSION EXPRESS

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

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Latest News

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

Sponsors Gear Up For a Smoother Process With CTIS but Must First Overcome Key Hurdles

Read the latest blog from our Pharmalex colleagues, Milena Shuytsova-Mircheva and Lisa Pascoe, who discuss the benefit of the Clinical Trial Information System (CTIS).     Companies have one year to

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It's time to raise your standard 

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