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Industry · Hospitals · Diagnostics · Pharma · MedTech

Healthcare & Life Sciences

Patient privacy and clinical continuity, not compliance theatre.

Hospitals, diagnostic chains, telemedicine platforms, pharma R&D groups, and medical-device manufacturers handle data and uptime requirements that punish theoretical security. We build programs that hold under HIPAA / HITECH, FDA pre-market cyber requirements, GDPR for clinical trials, and the realities of legacy clinical systems.

Who we work with

Audiences we routinely engage.

  • Hospital systems and IDNs
  • Diagnostic and reference laboratories
  • Telemedicine and digital-therapeutics platforms
  • Pharmaceutical R&D and clinical-trial sponsors
  • Medical-device manufacturers (Class II / III)

Frameworks & regulators

The standards your auditor will ask about.

We build to these as a starting point — not because the badges matter, but because the controls behind them earn the badges for free.

HIPAA / HITECHHITRUST CSFISO/IEC 27799FDA pre-market cybersecurity for medical devicesGDPR for clinical-trial dataGxP / ICH E6 (R3)ABDM (India)

Common engagements

What we typically run for clients in this sector.

01

PHI flow mapping and DLP rollout

02

Medical-device penetration testing and threat modelling (FDA-aligned)

03

Telehealth platform security and code review

04

HITRUST CSF implementation and certification

05

Ransomware-readiness programs for clinical operations

Operating in Healthcare & Life Sciences?

Tell us the regulator deadline, the audit cycle, or the incident on your mind. We'll come back with a scoped engagement that maps to your obligations and your budget.

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