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Text Content

 * Home
 * Our Services
   
   OUR SERVICES - ACCELERATING CLINICAL TRIALS.
   
   --------------------------------------------------------------------------------
   
   Open Data in Life SciencesData Standards Governor Synthetic Health
   DataTrialTwin - Clinical Trial Simulator Software-defined Reality
   
   FOLLOW US

 * Tech Partner Program
 * Events
 * Trade Shows
 * About Us
 * Shop

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 * +1 (650) 555-0111
   Contact Us

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 * 

 * 
    * Home
    * Our Services
    * Tech Partner Program
    * Events
    * Trade Shows
    * About Us
    * Shop

 * +1 (650) 555-0111

Contact Us


REDUCE PROCESSES. INCREASE PROGRESS.


NIHPO works with Life Sciences companies frustrated with their current clinical
trial data management processes.


Contact Us

We’re obsessed with helping organizations in the Life Sciences space (sponsors,
CROs, regulators, and providers, among others) to accelerate the development and
approval of Clinical Trials.




At a time of shrinking development timelines and increased market pressures,
organizations in the Life Sciences space are spending enormous amounts of money
in point solutions that merely perpetuate the underlying inefficiencies of
current processes.




NIHPO offers customized solutions that accelerate the development and approval
of clinical trials. Our platform replaces Excel-based terminology management;
manual study build and EDC testing; and multi-stage SAS transformations.




There are many companies claiming their software improves clinical trial data
processes. The problem we see is that most of those tools are mere patches on
top of outdated, inefficient, originally paper-based processes. “Digital Paper”
is how a customer of ours puts it.




At NIHPO we’re building a platform that eliminates those inefficiencies and
manual processes from the start. Leveraging Open Data and our Data Standards
Governor to drive the creation of Synthetic Health Data to perform better
testing and validation of processes. All the way to TrialTwin™, our Clinical
Trial Simulator.




NIHPO also offers an innovative pricing model for all our services: flat fee per
trial per year. With no per-user license. Our tools are available for and usable
by all users inside a customers’ organizations.




And you may rightfully ask: can a small company like NIHPO actually
revolutionize the clinical data management space, competing against entrenched
multi-billion software behemoths?




We believe that over a 10-20 year horizon we can. We’re not looking for neither
a quick exit nor an IPO. See more About Us.



OPEN DATA IN LIFE SCIENCES

Do you need real data to train AI / ML models and to perform historical
comparisons?




Leverage our compilation of over 30 years of Open Data in the Life Sciences
space.




See more details



DATA STANDARDS GOVERNOR

Some organizations manage regulatory standards (including terminologies) with
Excel files, Sharepoint, and by searching across external websites.





Are your users frustrated with the lack of access to a single source of metadata
truth? We can help.




See more details



SYNTHETIC HEALTH DATA (DIGITAL TWINS)


Are you looking for  realistic, unencumbered health data for testing and
validation purposes?




We generate non-real (yet realistic) synthetic health data based on customers'
specific requirements.

See more details


TRIALTWIN™ - CLINICAL TRIAL SIMULATOR


Imagine being able to simulate a clinical trial even before FPI. Now you can.




We offer TrialTwin™, a trial simulation and validation solution using customized
Synthetic Health Data.




See more details



SOFTWARE-DEFINED REALITY

We combine Open Data plus our Synthetic Health Data capabilities into a
Geographical Information System (“GIS”) to programmatically build “Alternative
Realities.” On a nation scale.

These “Alternative Worlds” maintain the same patterns of reality.





See more details



CURRENT STATE OF CLINICAL TRIAL DATA MANAGEMENT


There are many problems with the current state of affairs:

* Many transformation through SAS macros

* Data issues identified very late

* Potential for human errors

* Significant labor costs





Source: NIHPO's consulting work for a large multinational pharmaceutical
company.


A METADATA-DRIVEN OPTIMIZED PROCESS


We're building a [Metadata-driven] platform

that leverages both [Open Data] and [Synthetic Health Data]

to accelerate the testing and validation

of end-to-end clinical trial data flows.





Source: NIHPO's proposed platform to accelerate clinical trials.

Take a look at our Clinical Trial Simulator platform for more details.




Contact us to schedule an introductory call to review your organization's needs.

At the end of the call we'll determine if NIHPO can be of service to your
organization.



PARTNERING: TOGETHER WE BRING MORE VALUE TO YOUR USERS


NIHPO's data (both Open Data and Synthetic Health Data) as well as our custom
software can all be easily integrated into your platform.

Please take a look at our Tech Partner Program details.


Contact us



QUICK LINKS

 * * Home
 * * Open Data in Life Sciences
 * * Data Standards Governor
 * * Synthetic Health Data
 * * TrialTwin - Clinical Trial Simulator
 * * Software-defined Reality
 * * Tech Partner Program
 * * Events
 * * Trade Shows
 * * About us
 * * Contact us
 * * Privacy Policy

ACCELERATING DECISION-MAKING IN LIFE SCIENCES

We’re obsessed with helping organizations in the Life Sciences space (sponsors,
CROs, regulators, and providers, among others) to accelerate the development and
approval of Clinical Trials.  




We have a proven track record of helping clients:

* use Life sciences-specific Open Data

* centrally manage standards and terminologies

* generate highly realistic synthetic health data at scale (Digital Twins)

* use fit-for-purpose synthetic data to validate processes

* simulate Clinical Trials, from study build to full EDC output


LET US HELP YOU

 * NIHPO, Inc.
   15625 NW 15 Avenue
   Miami, FL 33169 - USA
 * 
   
 * Sales@NIHPO.com
   
   
 * +1 (561) 777-2577

SOCIAL MEDIA


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