Cybersecurity In Medical Devices

Practical Advice For FDA’s 510(K) Requirements

As the healthcare industry increasingly relies on interconnected medical devices, ensuring their cybersecurity is paramount to safeguard patient safety and data integrity. This webinar delves into the essential components of the FDA's requirements and provides practical guidance for implementing robust cybersecurity measures in connected medical devices.

By attending you will receive practical advice for implementing cybersecurity in medical devices including:

• Secure product development framework (SPDF)
• Threat and risk assessments
• Validation and penetration testing
• Security architectures