Research identifies templates for patient consent and sample reuse in ECRAID-Base POS studies, suggesting streamlined procedures.
For the ECRAID-Base POS studies we developed PIF/ICF templates for three potential scenarios - When the study does not collect any samples When the study will reuse leftover samples collected during standard care (current record) When the study will collect additonal samples
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Shreedhar et al. (2026) studied this question.
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