Validating Configurable Interactive Response Technology Solutions for Clinical Studies

Life Sciences, Clinical Trials, Pharmaceutical,
  • Wednesday, February 20, 2019

In this webinar, the validation of an interactive response technology (IRT) solution built with configurable parameters will be explored. Traditionally, interactive response technology solutions require validation of each study-specific requirement to ensure proper implementation. With the prevalence of configurable interactive response technology solutions where the validation of each configurable parameter occurs within the product, the need for full validation of each requirement within a clinical study has lessened. This webinar will explore how to take advantage of configurations and how to verify them, thereby reducing the effort and timeline required for validation while still maintaining quality within each study.


Herag Frankian, Program Director, Enabled & Enterprise RTSM, Bioclinica

Herag Frankian joined Bioclinica at the beginning of 2017 and is currently the Program Director, RTSM responsible for managing the Bioclinica IRT Enablement program, which enables pharmaceutical and biotechnology companies as well as CROs to build interactive response technology systems in-house. Herag has 12+ years’ experience within the interactive response technology industry in various roles ranging from software validation, project/program management and implementation of study and product standards.

Message Presenter

Who Should Attend?

This webinar is suitable for managers, leads and other relevant job titles in the following departments:

  • Clinical supply
  • RTSM
  • Interactive response technology
  • Clinical trial
  • Clinical operations
  • Clinical outsourcing
  • Clinical technology
  • Data management

What You Will Learn

Join this webinar to learn: 

  • How to validate an interactive response technology solution
  • How to take advantage of configurable parameters
  • How to verify configurations

Xtalks Partner


Bioclinica is a global life sciences solution provider that utilizes science and technology to bring clarity to clinical trials – helping companies to develop new life-improving therapies more efficiently and safely. With hundreds of experienced scientific, medical, and domain experts, we bring unmatched insight across the development lifecycle of a trial. Bioclinica’s cloud-based offerings include medical imaging, cardiac safety, clinical adjudication, randomization and trial supply management, clinical trial management, electronic data capture and eSource, site and patient payments, pharmacovigilance, and a global network of investigative sites. To learn more, visit us at

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