Cybersecurity – IT security for medical devices
The regulatory framework for Cybersecurity (IT-security) of medical devices is set out in the section “General Safety and Performance Requirements” of the EU regulations MDR and IVDR. Standards and guidelines specify the requirements for implementation.
Participants will receive an overview of the regulatory-relevant standards and documents along with practical advice, methods, tools and valuable resources to support implementation of the requirements.
seminar content
- Meaning of key terms from the fields of information security, IT security, and operational security
- Cybersecurity requirements for medical devices based on applicable standards, laws, and guidelines
- Tips, methods, tools, and other useful resources for implementing the requirements
Costs
1-day in-house training: €3,890 (excl. VAT) for up to 10 participants
Includes seminar materials and certificate of participation; travel expenses additional
your trainer
Nilaykumar Patel MSc, Chief Quality Officer at contextflow GmbH & Co-Auditor at en.co.tec
Information about our trainers
Book now:
Please send your request to seminare@encotec.at or call us: +43 1 8863491 +43 1 8863491
