Industries · Pharma

GxP IT that holds up under FDA inspection.

Validated systems, electronic-record / e-signature workflows, and cold-chain monitoring with audit trails that survive any 483.

One breach can undo a decade of reputation.

15-minute assessment · No sales call required.

Built for the audits you actually face.

21 CFR Part 11

Electronic records + electronic signatures controls for FDA-regulated workflows.

GxP

Good manufacturing / laboratory / clinical practice control validation.

Pharma IT consulting · HIPAA, NERC CIP & TSA-aligned cybersecurity

Modernize without the downtime.