healthcare · FDA 21 CFR Part 11 · FDA 21 CFR Part 211 GMP · ICH E6 GCP
GxP / FDA 21 CFR Part 11 Pharma
Delete audit trail before inspection = automatic consent decree pattern
—KISA AI guidelines + PIPA
Regulatory exposure — commonly overlooked:
QA releases batch on AI recommendation without hash-chained record — batch recall insurance void. · Korea AI Basic Act emerging — early movers on receipt infrastructure win Samsung/LG supply chain.
TAM / Exposure
Every GMP facility globally · Part 11 is law today
Insurance lines
Product recall · Pharma E&O
Exhibit authority
Korea AI Basic Act Pack — GxP Electronic Records Integrity Pack