IVR/IWR

CTMS

EDC

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.

We 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 has a proven record of managing and reducing client costs effectively and efficiently, providing an efficient way to implement and maintain their clinical trial software such as EDC, IVR/IWR and CTMS.

• Reduce the time and cost testing

• Meet and improve project timelines.

• Promote new system enhancements into production in less time on a repeatable basis.

• Eliminate post implementation defects that cause costly rework

• Decrease QA and testing expenditures on subsequent system implementations.

• Low cost of entry

• A repeatable enterprise wide solution that creates quick results while having minimal client organizational impact.

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