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?

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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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PHLEXDMS

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

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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

How to Reduce Risk and Effort When Migrating a Trial Master File

Migrating Trial Master File (TMF) data is a fairly common occurrence, usually driven by one or more of the following scenarios: Implementing a new electronic Trial Master File (eTMF) system

Consistency: The Secret to Improving Quality and Efficiency in TMF Document Processing

Based on extensive work helping trial sponsors and Contract Research Organizations (CROs) implement Trial Master File (TMF) best practices, Phlexglobal’s experts repeatedly encounter teams struggling

Solved: Is Our TMF Missing More than We Know?

In a poll of nearly 100 TMF professionals during a recent Phlexglobal webinar, “Lowering your TMF Risk Temperature: Real-world Use Cases and Lessons Learned,” more than half of the respondents were

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