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Clinical Trial Events
SCOPE Summit for Clinical Ops Executives

Talk Biomarkers & Precision Medicine Trials · Quality & Monitoring · Digital Health Technologies

Leveraging AI to Codify Informed Consent

Wed, Feb 5, 2025 · 11:55 AM–12:25 PM EST Rosen Shingle Creek

About this session

Informed consent codification to determine permissions and restrictions to utilize biospecimens and data is a manual and time-consuming task, but essential to ensure compliance and uphold commitments to participants. To increase efficiency and speed, BMS has developed an innovative AI tool to assist in IC Codification. The tool can identify relevant IC documents, scan and assess restrictive language to inform sample storage for clinical trial samples, and provide outputs to inform expedited reviews.

Speaker

  • Cristin Freeman

    Head, Informed Consent Management · Bristol Myers Squibb

    Speaker