Key benefits
- Understand the cybersecurity requirements and test standards for medical devices and IVDs in the EU and US
- Gain insights on the secure development process and discover best practices and industry standards for integrating cybersecurity measures
- Manage cybersecurity risk effectively to identify, assess and mitigate potential cyber threats
With the rapid integration of technology and connectivity in healthcare, medical and in-vitro diagnostic (IVD) devices are increasingly exposed to cyber threats that can impact patient safety and product performance.
In this on-demand session, we explore the critical topic of cybersecurity in the context of medical and IVD devices to ensure their safety and integrity in this ever-evolving digital age.
Gain practical insights on cybersecurity risk management, secure development process and explore methodologies to identify, assess, and mitigate potential threats to your medical and IVD products. You’ll also learn about key regulatory requirements and compliance standards in both the EU and US.
To view the webinar, fill in the form now.
Our webinar will tackle these points, focusing on
- Overview of medical product development life cycle
- Cybersecurity landscape in medical IoT products
- How regulators react to cybersecurity incidences
- TÜV SÜD’s interpretation on regulatory requirements for cybersecurity in the EU and US
- Cybersecurity risk management
About the speaker
Marwan Samir
Senior Penetration Tester, TÜV SÜD
