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ERT’s SITEpro® Tablet is Authorized to Administer Key Respiratory Quality of Life Assessments
Date:7/10/2013

PHILADELPHIA, PA (PRWEB) July 10, 2013

ERT, a leading global solution provider for high-quality patient safety and efficacy endpoint data collection, today announced that it is authorized to provide validated, electronic versions of commonly used health-related Quality of Life (QoL) questionnaires on SITEpro® Tablet -- its patient data collection system for use at the investigative site. The questionnaires, developed by Professor Elizabeth Juniper, are considered the gold standard for measuring QoL among patients in clinical trials of medical products being developed for the treatment of asthma and rhinoconjunctivitis.

SITEpro enables biopharmaceutical companies to capture important Clinical Outcome Assessments (COAs) - including patient, clinician, and observer reported outcomes (PROs, ClinROs, and ObsROs) -- via an easy-to-use electronic tablet. Patients and site personnel use SITEpro during investigative site visits to respond to questionnaires about their health and quality of life as they participate in clinical trials of new medical products. The authorization will give biopharmaceutical companies confidence that SITEpro is an effective tool for measuring quality of life as they develop medical products for the treatment of asthma and rhinoconjunctivitis.

In order to receive authorization, the screen shots for SITEpro Tablet were formatted to be as similar as possible to the validated paper versions of the questionnaires. In addition, ERT successfully demonstrated that patients were able to use, understand, and complete all three questionnaires on both SITEpro Tablet 10” and SITEpro Tablet 12” data collection devices. The specific assessments that have been authorized for SITEpro Tablet administration include:

  •     Asthma Control Questionnaire (ACQ)
  •     The standardized version of the Asthma Quality of Life Questi
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