Product/Service

Site Based ePRO

Source: Invivodata
invivodata's innovative in-clinic solution, SitePRO®, combines clinical science with technology to increase efficiencies in site-based patient reported outcomes (PRO) data collection in clinical trials.

invivodata's innovative in-clinic solution, SitePRO®, combines clinical science with technology to increase efficiencies in site-based patient reported outcomes (PRO) data collection in clinical trials. SitePRO collects accurate PRO data to deliver error-free data directly from the patient and eliminates costly transcription errors, out-of-range entries, illegible responses, and double data entry associated with paper-based studies.

Proven Software Delivers Confidence
In use since 2004, SitePRO is the industry's only site-based ePRO solution to have collected primary efficacy data in support of a successful New Drug Application (NDA). SitePRO reduces risk and delivers confidence. Data quality and accuracy have been proven in dozens of trials.

Clinical Trial Role
Benefit
Sponsors

  • Improves efficiency by collecting clean, in-range, legible data
  • Eliminates missing and inaccurate data which is inherent with paper-based PROs
  • Reduces study timelines by eliminating the need to transcribe hand-entered PRO data

Sites

  • Reduces the amount of paper that needs to be managed and stored at the site
  • Supports diverse patient demographics and accessibility requirements, thereby increasing the pool of patients available for enrollment

Patients

  • Decreases time to complete in-clinic assessments through a user-friendly interface
  • Provides accessibility features based on patient population including enlarged fonts and oversized stylus
  • Easy-to-use patient interface translated into the local language eliminates patient confusion