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HomeCurrent/Future EventsWebinar - Understanding Landscape of Medical Device Cybersecurity Regulations

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Webinar - Understanding Landscape of Medical Device Cybersecurity Regulations

When:
Tuesday, March 17, 2020, 8:15 AM until 10:00 AM
Additional Info:
Event Contact(s):
ORCA Admin
Category:
Webinar
Registration is closed
Payment In Full In Advance Only
RSVP by Monday, March 16 2020

Meetings and webinars are scheduled on Pacific Standard Time or Pacific Daylight Time, whichever applies.

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PAID FEES ARE NON REFUNDABLE.

For webinar events, payment is REQUIRED at the time of registration.
Capacity:
100
No Fee
$60.00

The link to the webinar is intended for the registered person ONLY and should not be shared.
All attendees MUST be registered.
This webinar will be recorded.

THIS IS A TUESDAY MEETING




TOPIC:
Understanding Landscape of Medical Device Cybersecurity Regulations


TOPIC DESCRIPTION:
FDA and other regulators are continuing to issue new guidance on Cybersecurity requirements for Medical Devices. Key provisions of these regulations are being adopted by MDR and IVDR governing bodies to help shape new regulations for Europe as well. During this session, you will gain a deeper understanding of the evolving Cybersecurity requirements for Medical Devices as issued by the FDA and other regulators.

The discussion will include a review of the requirements from:

• October 2018 draft FDA Guidance “Content of Premarket Submissions for Management of Cybersecurity in Medical Devices
• A review of the International Regulatory Landscape in Cybersecurity
• Recent developments of Cybersecurity Standard

Come engage with professionals from your local regulatory community for an interactive presentation on cybersecurity requirements for Medical Devices.


SPEAKER:
Christopher Beeman


SPEAKER BIOGRAPHY:
Chris Beeman is the Medical Device Software and Cyber Practice Lead for Emergo by UL. This service is designed to develop, support and deliver risk mitigation solutions for IoT or software enabled medical devices, so that manufacturers, can do what they do best, innovate.

WHO: Clinical, regulatory, quality, manufacturing and legal

Attendance at this meeting may be applied as 1.5 points towards RAC re-certification