USGrantIn forceModel providersDeployers

FDA Awards Cognita Imaging $1.29M to Validate LLM-as-a-Jury Evaluation Across 1 Million Radiology Reports

美国FDA向Cognita Imaging拨款129万美元用于LLM作为陪审团评估百万级放射报告
FDA·Published 2026-09-16·Checked by 管理员 on 2026-09-18

The U.S. Food and Drug Administration (FDA) awarded Cognita Imaging, Inc. (a wholly owned subsidiary of Mosaic Clinical Technologies, Inc.) a $1.29 million research contract to pioneer new methodologies for evaluating autonomous, generative AI radiology reports. The 18-month contract, effective June 22, aims to validate the LLM-as-a-Jury evaluation method across 1 million radiology reports.

What it means for you

• Company Obligations: Cognita Imaging must complete the development and validation of an LLM-as-a-Jury evaluation method for 1 million radiology reports within 18 months, meeting FDA research requirements.

What to do

ComplianceMonitor the FDA's research progress on AI radiology report evaluation standards and assess its impact on existing products.
ProductEvaluate the LLM-as-a-Jury technical solution and explore its potential applications in radiology report quality control and efficiency improvement.

Key dates

2026-06-22In force
2026-09-16Published

Source documents

Coverage

Stories in the feed
Editorial summary, not legal advice; dates and status follow the original document. · Report a correction