Attend from anywhere: 25 – 26 March 2025, 9 am – 5 pm ET
This interactive virtual workshop will provide crucial insights into navigating global cybersecurity regulations and developing effective strategies to strengthen your submissions and compliance processes.
After completing this two-day workshop, you will be able to:
Understand cybersecurity expectations from US, EU, Australian, Canadian, and Japanese health authorities
Build robust cybersecurity content and reduce deficiencies in premarket and postmarket submissions
Equip your technical teams with the tools to implement regulatory requirements into your product security program
Speakers
Michelle Jump, CEO, MedSec, responsible for providing strategic leadership, training, and advisory services to the medical device industry in cybersecurity compliance, global regulations, standards, product security program development, and security risk management
Justin Post, Policy Analyst (Cybersecurity), Center for Devices and Radiological Health (CDRH), U.S. Food and Drug Administration (FDA)
Nastassia Tamari, Division Director for Medical Device Cybersecurity within the Division of Medical Device Cybersecurity (DMDC), housed within the Office of Readiness and Response (ORR) in the Office of Strategic Partnerships and Technology Innovation (OST) in FDA CDRH
Ensure your organization is well-prepared for the evolving cybersecurity landscape in medical device regulation.
