ClinPlus® Releases Clinical Trial Suite with fully Unified EDC IWRS and CTMS solutions

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ClinPlus is now the only software company with unified EDC, IWRS, CTMS, eTMF, SAS Reporting for BioStats teams, Medical Coding for dictionary management, user defined dashboards and Ad-Hoc reports.

ClinPlus announces the release of ClinPlus eClinical Version 3.2 that includes many important features to increase efficiencies for Clinical, Site Research, and Data Management teams across all modules in the eClinical suite. These enhancements improve key decision making, data transparency, and reduces data redundancies across clinical teams.

Significant 3.2 Features include:

  • Unification of EDC and IWRS.
  • Now includes CDISC CDASH eCRF Library.
  • Now includes SDTM Codelist Library.
  • Improved Data Imports/Exports for EDC Data.
  • Improved printing of Patient Case Books.
  • Improved printing of annotated and blank eCRFs.
  • Many additional usability and performance enhancements.

“Our platform is adaptable, user configurable, SaaS based for leveraging six-week deployments, and modules can be licensed separately or together. “Having all solutions on one unified, single sign on platform will decrease cost and eliminate the need for point to point integrations and separate user licenses for each module.”

Jessica Schell,
Director ClinPlus Division

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Anju ClinPlus, LLC

Jessica Schell

Anju ClinPlus, LLC

Bob Borysko

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