Webinar “Cyber Resilience Act: Challenges Regarding the Transition Period Until 2027”
Discover the challenges of the transition period and where companies are already under pressure. Learn how to proactively plan regulatory, technical, and organizational measures to mitigate risks. Get a concise overview of deadlines, obligations, and concrete next steps for CRA preparation.”
Webinar overview
Date:
22 September 2026
Time:
12:00 – 12:45
Language:
German
Location:
Online
Cost:
Free of charge
Overview
Course Objectives
By the end of this webinar, participants will be able to:
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Understand the key requirements and objectives of the Cyber Resilience Act
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Realistically assess the significance of the transition period until 2027
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Identify critical action areas such as product development, vulnerability management, and documentation
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Define initial concrete measures to align their company with CRA compliance
Target Audience
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Manufacturers of products with software
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Product managers, development, and engineering teams
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Quality, compliance, and regulatory affairs managers
Speaker
Thomas Schwendinger
Head of Regulatory Affairs and Quality Management
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10 years of experience in medical device development
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Bachelor’s in Systems Engineering, NTB Buchs, specialization in Mechanics
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Master’s in Energy Engineering, FHV
Adrian Gerber
Senior Regulatory Affairs & Quality Manager
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Regulatory Affairs and Quality Management
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4 years of experience in medical device development
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Bachelor’s in Medical Engineering, Lucerne University of Applied Sciences/FHZ