Healthcare
The auditor asks. You need to be able to prove it.
We implement security so it holds up to audits, and run your systems so every change is traceable.
What is different in your industry
In pharma, medical devices and healthcare logistics, every change to a system has to be documented and traceable. Auditors don't just want to know that it's secure, they want to know how you prove it.
What applies to you. And what we do about it.
Auditors do not want to hear that it is secure. They want to see it. We run your systems so every change is in the audit log, and implement security so the evidence comes with it.
- NIS2
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For many companies in the healthcare sector.
Scope analysis inside the Assessment. Then measures implemented, documented, and reported to management.
- GMP Annex 11
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Computerized systems in pharmaceutical manufacturing.
Every change to a system we operate is in the audit log in your environment: who, what, when.
- MDR
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The EU Medical Device Regulation.
- KRITIS regulation
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Germany's rules for critical healthcare facilities.
Hardening and attack detection in your environment, every measure with evidence for the audit.
Let's talk about your audits.
30 minutes with someone who knows your regulatory environment.