PLOS Global Public Health (Jan 2023)

From biorepositories to data repositories: Open-access resources accelerate early R&D and validation of equitable diagnostic tools.

  • Roger Peck,
  • Helen L Storey,
  • Becky Barney,
  • Shirli Israeli,
  • Olivia Halas,
  • Deborah Oroszlan,
  • Shiri Brodsky,
  • Neha Agarwal,
  • Eileen Murphy,
  • Mariana Sagalovsky,
  • Jessica Cohen,
  • Elizabeth Trias,
  • Aaron Schutzer,
  • David S Boyle

DOI
https://doi.org/10.1371/journal.pgph.0002044
Journal volume & issue
Vol. 3, no. 8
p. e0002044

Abstract

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Diagnostics are critical tools that guide clinical decision-making for patient care and support disease surveillance. Despite its importance, developers and manufacturers often note that access to specimen panels and essential reagents is one of the key challenges in developing quality diagnostics, particularly in low-resource settings. A recent example, as the COVID-19 pandemic unfolded there was a need for clinical samples across the globe to support the rapid development of diagnostics. To address these challenges and gaps, PATH, a global nonprofit, along with its partners collaborated to create a COVID-19 biorepository to improve access to biological samples. Since then, the need for data resources to advance universal rapid diagnostic test (RDT) readers and noninvasive clinical measurement tools for screening children have also been identified and initiated. From biospecimens to data files, there are more similarities than differences in creating open-access repositories. And to ensure equitable technologies are developed, diverse sample panels and datasets are critical in the development process. Here we share one experience in creating open-access repositories as a case study to describe the steps taken, the key factors required to establish a biorepository, the ethical and legal frameworks that guided the initiative and the lessons learned. As diagnostic tools are evolving, more forms of data are critical to de-risk and accelerate early research and development (R&D) for products serving low resource settings. Creating physical and virtual repositories of freely available, well characterized, and high quality clinical and electronic data resources defray development costs to improve equitable access and test affordability.