We proactively help ATMP developers and manufacturers, technology suppliers, hospitals, clinics, and related healthcare service providers protect their assets, technology-data, and products from cyberattacks — always up to date with EU and German regulations.

Cybersecurity in healthcare is no longer optional. A broader range of organizations face additional strict requirements in Information Security with liability for non-compliance and increasing risks for cyber criminality.
At cellerata, we address these challenges through a clear, step-by-step approach:
- Assessment: initial cybersecurity check to identify gaps and risks
- Definition: action items aligned with your specific priorities and partner needs
- Execution: operational guidance and hands-on project delivery
- Implementation: organizational integration and audit-ready documentation
This way, we want to strengthen organizational resilience while ensuring compliance with EU and German regulations with a special focus on small entities as niches which may not be sufficiently protected.

Why It Matters
Healthcare and pharmaceutical organizations must manage highly sensitive patient, product, and process data. A single cyberattack can block access to infrastructures, data and networks — with devastating consequences. Imagine a severely ill patient or even a child who cannot be treated because essential data, documents, or a time-sensitive therapy product is suddenly unavailable.
The risks are especially high in:
- Production and supply of sensitive, high-end therapeutics: pharma, biotech, manufacturers, suppliers, and labs
- Healthcare delivery: diagnostics, administration of innovative medicines, patient treatment, and follow-up care
At cellerata, we help you reduce these risks by:
- Ensuring information security with state-of-the-art protection
- Protecting critical (very important and important) infrastructures and, in particular, the interfaces connected to KRITIS environments
- Creating and evaluating audit-proof documentation and transparent reporting
- Supporting clients in managing their liability and responsibility for products, services, and patient safety
Our mission in a nutshell:
Make information security achievable – asap – especially for resource-constrained organizations, focus in the healthcare sector.
How cellerata safeguards Information security

Information Security Assessments (IS / ISMS)
Identify gaps and build a clear roadmap for cyber protection, partnered with pm-praxis.de
- Gap analysis vs. NIS-2, ISO/IEC 27001, BSI IT-Grundschutz
- Risk management with tailored, action-oriented plans
- Compliance roadmap with measurable milestones
- Set up your information security project and build the right team for implementation

Project Management for Information Security
Lean project execution tailored to SMEs and healthcare organizations.
- Integration with existing IT systems and quality frameworks
- Transparent planning, stakeholder alignment, and reporting to management
- Readiness for audits, inspections, and authority engagement
- Continuous updates and check-ups with recommendations
- Support in emergencies and during security audits
We take actions for your confidence
If you are unsure about cybersecurity in your organization, we are here to help. We start with an initial assessment and provide you with a tailored information security management approach that fits your needs.
Why Work With Us?
Information security in healthcare is as critical as pharmaceutical manufacturing, because both directly protect patient safety. At cellerata, we combine regulatory knowledge with hands-on project execution to deliver lean, pragmatic, and compliant solutions.
Healthcare expertise
Experience with hospitals, clinics, SMEs, specialized centers, and ATMP developers
Lean and pragmatic approach
Faster and more cost-efficient than relying solely on internal resources or CDMOs
Trusted partnerships
Close collaboration with pm-praxis for healthcare projects and DriveLock for technical cybersecurity solutions
National compliance focus
Information security projects aligned with German regulations, with a clear understanding of EU requirements
Smooth transfer support
efficient handover from developers to CDMOs, or from international organizations (e.g. US) into Germany and Europe
Full lifecycle coverage
From initial assessment to implementation, documentation, and audit support