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End-to-end simulation of clinical trials

What is Trial TwinTM?

Database-driven software platform that generates realistic, yet Synthetic Health Data.

We value your time

TrialTwinTM 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.
Faster start-up
Test and validate processes before First Patient In. Easily accommodate protocol changes. Unrestricted synthetic data at large scale.
Fit within existing processes
Helps drive faster Operational Innovation. We accelerate all data handling and bureaucratic processes, so you can focus on the actual Science.
Validate Processes
We help medical device and pharma companies to meet regulatory requirements for system validation and verification. Synthetic Health Data ensures all systems and processes are fully tested before going into production.
Realistic data
Data cannot be totally random, nonsense. Synthetic Data has to be representative of the “Patterns of Reality”.

Full compliance

Our synthetic data has no privacy regulations nor any re-usability limitations. Totally compliant with GDPR, HIPAA...
Each anonymization or model-generation tool has an implied de-anonymization risk factor.
Our approach is more flexible, scalable and easier to implement than existing synthetic data generators. In addition, Synthetic Health Data provided by TrialTwinTM has absolutely no risk of ever becoming “de-anonymized” as there are no “real” people behind the data.

What is
Trial TwinTM

Database-driven software platform that generates realistic, yet Synthetic Health Data.
Faster start-up
Test and validate processes before First Patient In. Easily accommodate protocol changes. Unrestricted synthetic data at large scale.
Fit within existing processes
Helps drive faster Operational Innovation. We accelerate all data handling and bureaucratic processes, so you can focus on the actual Science.
Validate Processes
We help medical device and pharma companies to meet regulatory requirements for system validation and verification. Synthetic Health Data ensures all systems and processes are fully tested before going into production.
Realistic data
Data cannot be totally random, nonsense. Synthetic Data has to be representative of the “Patterns of Reality”.

Full compliance

Our synthetic data has no privacy regulations nor any re-usability limitations. Totally compliant with GDPR, HIPAA...
Each anonymization or model-generation tool has an implied de-anonymization risk factor.
Our approach is more flexible, scalable and easier to implement than existing synthetic data generators. In addition, Synthetic Health Data provided by TrialTwinTM has absolutely no risk of ever becoming “de-anonymized” as there are no “real” people behind the data.
CREATOR: gd-jpeg v1.0 (using IJG JPEG v62), quality = 35

Top-of-the-line partners

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What we stand for?

Mission
We aim to help the world through our expertise in Software and IT applied to life sciences. Our work on progressively optimizing processes in the Pharma space is already improving processes among some of the largest names in the industry.
Vision
We are becoming a standard in reducing Clinical Trial Building Time, automating CRF Validation & Verification, validating and stress-testing your internal tools and emulating real world data into your Trial through the usage of Synthetic Data.
People
Our team is led by an entrepreneurial and philanthropic spirit. In TrialTwin we all share this humanitarian perspective and passion for the business of software and IT in the Pharma field. We achieve low costs by using agile, fast and simple methodologies, supported by open standards and open data, while maintaining customer-need driven products.

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    Come and visit our quarters or simply send us an email anytime you want. We are open to all suggestions from our audience.
    Address
    NIHPO, Inc.
    15625 NW 15 Ave.
    Miami, FL 33169
    Email
    info@nihpo.com
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