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Pharmaceutical sector

Data integrity, GMP validation and processes that do not permit uncontrolled changes: security must fit within that framework.

The environment

Production, laboratory, serialisation and utility systems support validated processes and sensitive records. Changing without impact assessment is not an option, but neither is leaving legacy systems and access uncontrolled.

How we work here

We document assets and flows, coordinate each test with quality and production and turn findings into traceable measures. We combine OT assessment, segmentation, access control and testing in authorised environments.

Applicable regulations

NIS2 covers the manufacture of certain pharmaceutical products and the health sector. Measures must coexist with GMP, data integrity and validation; IEC 62443 is the technical reference for the industrial environment.

Titanium · Legal information
Titanium · Legal information
Titanium · Legal information