Webinar: Medical Device Risk Assessments - Cybersecurity, Compliance & Patient Safety
· On-demand
Synopsis
This webinar focuses on the critical role of risk assessments in medical device cybersecurity. It delves into the processes and considerations necessary to identify, evaluate, and mitigate cybersecurity risks throughout the medical device lifecycle. The discussion will cover how effective risk assessments contribute to regulatory compliance and, most importantly, safeguard patient safety by preventing cybersecurity vulnerabilities from impacting device functionality and data integrity.
Key takeaways
- Understand the key components of a comprehensive medical device cybersecurity risk assessment.
- Learn how to integrate cybersecurity risk assessments with existing quality management systems, aligning with standards like ISO 14971.
- Explore strategies for achieving regulatory compliance with frameworks such as FDA Section 524B and IEC 62304 through robust risk assessment practices.
- Discover methods for identifying and prioritizing cybersecurity threats and vulnerabilities specific to medical devices.
- Gain insights into how proactive risk mitigation directly enhances patient safety in the context of connected medical devices.
Ready when you are
Get FDA cleared without the cybersecurity headaches.
30-minute strategy session. No cost, no commitment - just answers from people who've shipped 250+ submissions.