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Sharp’s IRT System will be the main entry point for subjects in your clinical trial. Our IRT System has many options for enrollment as shown below:

  • Screening and Screening Failures
  • Randomizations
  • Cohort and Cohort Management
  • Early Terminations
  • Subject Completion

Sharp IRT forms can be configured to capture any trial data items required for Screening, Randomization, and other Trial visit activities.  Trial data can also integrate with EDC and other connected eClinical systems.

Related Resources

Sharp has received Investigational Medicinal Product (IMP) & Wholesale Distribution Authorisation (WDA) licensing approvals to support clinical activities from its facility in The Netherlands.
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Great to meet new and familiar faces at Pharma & Device Packaging & Labelling Europe 2019 today in Munich. Connect with Scott Forde to learn more about our state of the art facility in Rhymney. @ArenaIntPharma https://t.co/dxRZUgmZVS

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Are you attending Clinical Innovation Partnerships in Berlin next month? Connect with the Sharp team to learn more about our high-speed bottling capabilities. https://t.co/iUbRiX2S68

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