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SCADA Compliance for Life Sciences: 21 CFR Part 11 Electronic Records & Audit Trails

Designing validated SCADA systems for pharmaceutical and biotech manufacturing: ALCOA+ data integrity principles, dual-authorization electronic signatures, and tamper-proof audit trails.

  • Part 11 mandates that electronic records and signatures carry the same legal standing as paper records and wet ink.
  • Every setpoint change, batch start, and alarm acknowledgment must log timestamp, user identity, old value, new value, and change reason.
  • Audit trail databases must be encrypted and write-once, preventing alteration even by database administrators.

Flow Ctrl Tech Engineering: Turnkey industrial automation, PLC programming, SCADA development, HMI, fieldbuses, and IIoT architectures. Contact our engineering center at [email protected] or phone +91 91110 91005.