PhlexTMF Express is an ideal solution for companies seeking best-of-breed eTMF software to improve inspection-readiness and productivity, without the need for customization.
Built by Phlexglobal, the global authority in Trial Master File best practices, PhlexTMF Express incorporates our “gold standard” eTMF configuration out of the box – so you can get up to speed quickly and with confidence.
Our customers are usually up and running with PhlexTMF Express in 7-10 days, since the software has already been configured to Trial Master File best practices.
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Phlexglobal's purpose-built, expert eTMF software |
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Digital document processing for active studies |
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Flexibility from per-study pricing |
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AI-assisted Indexing |
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Phlexglobal's 'Gold standard' best practices configuration, processes, and services |
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Quality Control (QC) |
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TMF Reference Model Structure |
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PhlexTMF mobile scanning and classification app (iOS & Android) |
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User management & study set-up |
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Query set-up and management |
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eLearning training for users |
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Audit and inspection support |
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Automatic software upgrades |
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Read-only viewing for closed studies |
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Global support |
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Completeness reporting |
Have more complex requirements such as multiple TMF structures or unique processing requirements? Check out
PhlexTMF Enterprise
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
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
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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