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Researchers can only reuse clinical samples for future studies if participants give informed consent for them to do so. Most scientists do not get this consent.
The biopharmaceutical industry is always looking for ways to speed up clinical trial timelines while maintaining patient safety and compliance with regulatory guidelines.
Academic biobanks support preclinical and translational research by collecting, storing, analyzing, and distributing biological samples and associated data to academic and industry researchers.
Repurposing patient samples for multiple non-interventional research studies can maximize sample value and help address the industry-wide problem of patient recruitment.