TrïalTwïn - Simulation of Clinical Trials

NIHPO’s TrialTwin™ platform is a “No Code”, integrated, centralized trial simulation and validation solution. TrialTwin™ generates customized, realistic and scientifically-accurate Synthetic Health Data. This synthetic data accelerates the development and validation of clinical trial software and processes.

TrialTwin™ gives sponsors total control over the ingestion, storage, and processing of their study data. Sponsors can now easily switch vendors (EDC, CROs, labs, etc.).

The TrialTwin™ Platform helps all staff roles at life sciences companies to reduce the time it takes to

  • design,

  • develop,

  • test,

  • validate, and

  • obtain regulatory approval for

new drugs and medical devices.

Current State

  • Multiple data transcoding processes

  • Very labor intensive, requiring custom scripts

  • Different data consumers see data at different times

  • Difficult to run early test and validation of data analysis

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With TrialTwin

  • Eliminate data transcoding processes

  • Reduce labor intensive processes, no custom scripts

  • All data consumers access updated data at same time

  • Run test and validation of data analysis before First Patient In

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TrialTwin Video

This video describes the TrialTwin platform in detail.

Additional Videos

For background please watch this YouTube video for details on NIHPO’s concept of Software-defined Reality™

Also, please watch these related videos as well:

SynthPerson™ - A Realistic, Scientifically Accurate Synthetic Person

SynthPHR™ - Creating Synthetic Personal Health Records (“PHR”)

SynthTrial™ - Creating Synthetic Clinical Trial Data (CDISC SDTM)

Contact Us

NIHPO, Inc.

15625 NW 15th Ave

Miami, FL 33169-5601

Jose C. Lacal, CTO

+1 (561) 777-2577

Jose.Lacal@NIHPO.com