In this episode, we take an in-depth look at cybersecurity from a medical device perspective. Plantvision’s Henrik Fält Padoan sits down for a conversation with Jerker Åberg, who is responsible for Regulatory Affairs, Product Compliance, and Post-Market Surveillance at Getinge, Critical Care, in Solna. The conversation provides concrete insights into how regulations, standards, and practical implementation are interconnected, and why organization, expertise, and culture are often the biggest challenges. They also discuss the balance between transparency and security, how older products are managed in a new threat landscape, and why future requirements will demand faster updates and a more proactive approach. An episode for those who want to stay one step ahead in an increasingly connected medtech landscape.