Building a Regulatory Risk Copilot with Databricks Agent Bricks (Part 1: Information Extraction)
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In July 2025, the US FDA publicly released an initial batch of 200+ Complete Response Letters (CRLs), decision letters explaining why drug and biologic applications were not approved on first pass, marking a major transparency shift. For the first time, sponsors, clinicians and data teams can analyze the industry through the agency’s own language about deficiencies across clinical, CMC, safety, labeling, and bioequivalence, via centralized, downloadable open FDA PDFs.

As the FDA continues to release new CRLs, the ability to rapidly generate insight from this and other unstructured data, and add to their internal intelligence/data, beco…

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