// by industry
Pharmaceutical & Life Sciences OT Security
OT cybersecurity for pharmaceutical and life-sciences manufacturing — protecting GMP process control, batch systems, and data integrity where a cyber event is also a compliance and patient-safety event.
In pharmaceutical and life-sciences manufacturing, the control system is also a quality system. GMP process control, batch execution, and the records they produce underpin product quality and patient safety — so a cyber event that alters a setpoint or a batch record is a data-integrity and compliance failure, not just an IT incident.
Hillstrong secures pharma OT with integrity and validation in mind. We baseline and segment process control and batch systems, protect data integrity against tampering across the ALCOA+ and 21 CFR Part 11 requirements, and plan every change to fit validated-system change control.
Resilion tracks the program against your quality and compliance obligations, so security evidence stands up to an inspection the same way the rest of your GMP record does.
Frequently asked questions
- How does OT security intersect with GMP and data integrity?
- In pharma, process control and batch records underpin product quality and patient safety. A cyber event that alters a setpoint or a record is a data-integrity and compliance failure (ALCOA+, 21 CFR Part 11), so security controls must protect integrity without breaking validated-system discipline.
- Can security work be done on validated systems?
- Yes — carefully. We plan changes to fit validated-system change control and GMP requirements, so segmentation and monitoring get implemented without invalidating the system or the record.
See Resilion on your fleet
Book a 30-minute demo. We will show how Resilion turns your existing assessments into a program you can run and prove.