Comment from Centre for Commercialization of Regenerative Medicine (CCRM)

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Summary: CCRM, a business entity, supports the draft guidance but requests specific clarifications and improvements to ensure consistent, risk-based decision-making. They advocate for clearer definitions regarding NGS sensitivity, integration site analysis, and sample selection to improve regulatory efficiency and scientific rigor.
Please refer to the attached communication letter "CCRM-OmniaBio Comments_FDA Draft Guidance_Docket No. FDA-2026-D-1255_13Jul2026".

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