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 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.

Deploy 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

CONTACT