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Food and Drug Administration (FDA) is the primary regulatory body in the United States responsible for ensuring the safety, efficacy, and quality of medical products
Baseline assessment should include evaluation of renal function, particularly for direct oral anticoagulants (DOACs) which require dose adjustments in renal impairment
Most clinical trial data supports use of 3 to 6 months without long-term safety concerns
Additionally, eryptosis offers a higher reproducibility, easier quality control, better data precision, and the opportunity to identify changes in eryptosis signaling pathways at the suberyptotic concentrations of nanomaterials
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