As healthcare becomes increasingly connected, medical device cybersecurity is no longer an IT issue — it is a patient safety imperative. In this expert discussion, three leaders at the intersection of regulation, standards, and innovation explore why cybersecurity must be embedded into the DNA of medical device design from day one.
What You’ll Learn
- Standards and Innovation — Raising the Bar
- Purpose Driven Functionality & Protecting Patients
- Predictability & Security in Procurement
- Designing with Standards from the
Start
- Medical Devices in Patient Care Settings
- FDA’s VEX Data & Quality Management Systems
- Cybersecurity = Patient Safety
- Be Proactive. Participate. Lead.
Featuring:
- Naomi Schwartz, Vice President, Regulatory Strategy, Medcrypt
- Elizabeth Baker, PhD, Professor of Information Systems at Virginia Commonwealth University and THMT Academic & Research Integrity Oversight
- Maria
Palombini, Director, Healthcare & Life Sciences Global Practice Lead, IEEE Standards Association
Listen & Watch
Access the full video and audio at the DOI: https://doi.org/10.30953/thmt.v11.696
Stay ahead of regulatory expectations. Design smarter. Protect patients.
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