PAREXEL® Informatics
Perceptive Informatics™ is now PAREXEL® Informatics. The new name reflects our new role as the eClinical technologies part of PAREXEL. It’s great for us and our clients because now our advanced Perceptive MyTrials® platform is integrated throughout your development journey to accelerate every phase.

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For biopharmaceutical companies interested in technology solutions designed to improve how you perform clinical trials, control and share data, track and report patient outcomes, and manage regulatory information, visit the PAREXEL website.

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For CROs and other partners interested in leveraging the Perceptive MyTrials® eClinical platform to complement and enhance service offerings, visit the Perceptive Partner Program website.

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Perceptive MyTrials®

One login. One location. All the information you need at your fingertips. Perceptive MyTrials gives you single-point access to a suite of fully integrated applications, data, and information associated with clinical trials and programs.

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Study Management & Monitoring

Clinical trials constitute the single most expensive component of the entire drug development process. Find out more about our proven CTMS solutions for biopharmaceutical companies of all sizes.

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Clinical Data Management

Read more about our DataLabs® EDC solution. It is uniquely focused on streamlining the entire process starting from study design all the way to collection, management and reporting of clinical trial data.
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ePRO Products

Read more about our solution for patient self-reported data, quality of life assessment, patient recruitment, symptom, safety information, and medical compliance monitoring.
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Randomization & Trial Supply Management

Read more about our web-based ClinPhone RTSM solution for automated randomization and supplies management.
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Medical Imaging

Find out why PAREXEL Informatics is known for its impressive, sustainable track record of successfully applying and managing medical imaging in clinical trials.
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Regulatory Information Management

Learn more about LIQUENT InSight® solution, the only end-to-end, integrated Regulatory Information Management (RIM) platform on the market today, delivering powerful submission planning, publishing, viewing, and registration management.

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