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
obtain regulatory approval for
new drugs and medical devices.
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
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
This video describes the TrialTwin platform in detail.
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)
15625 NW 15th Ave
Miami, FL 33169-5601
Jose C. Lacal, CTO
+1 (561) 777-2577