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What we do RealityCorp provides quality assurance,
data validation and testing for clinical trial software. Our
service is provided as a Software as a Service (SaaS) solution.
Our clinical trial testing and validation automation ensures that
our clients not only improve their time to market but their quality as well.
Software validation is a main driver for our clients since FDA
regulations require our clients to do it, RealityCorp's
methodology makes that task faster, better and safer. Our software product
and Clinical Trial Services Methodology (ClinTest) enables us to quickly test and validate regulated
systems (eg., IVR, IWR, CTMS, EDC, etc.). Our clinical trial services testing and validation
solution supports healthcare, pharmaceutical and bio-pharmaceutical organizations who are
trying to reduce their risk exposure, decrease the cycle time from development
to implementation and reduce costs in a highly regulated environment that is resource
and time constrained.
How we do itWe are able to deliver tremendous
quality assurance and testing value
to our clients by utilizing our extensive industry experience in continuing to enhance the proven success
with our Clinical Trial Service Methodology, proprietary quality assurance and testing software, and special techniques that we
have learned to effective deploy.
RealityCorp creates, deploys and builds validated automation
solutions using various products and tools including Microsoft Visual Studio and
hosted on Microsoft Windows Server. Our staff utilizes and takes full advantage
of Microsoft Office suite to present custom reporting and support solutions to
our clients.
Mission StatementDeploy reliable
technology to accelerate drug development, validate results and have an impact
on the health of mankind
Core Beliefs
1.
Integrity
2.
Consistent learning
3.
Commitment to Quality
4.
Continuous Process Improvement
Value Proposition
Our
automated process:
1.
Accelerates the drug deployment
process
2.
Provides for reliable delivery of
accurate data
3.
Intelligently mitigates risks
4.
Provides fast and agile inclusion of
amendments
5.
Increases the probability of a
successful result
6.
Minimizes human error
7.
FDA Compliant

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