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Medical Technology in the Digital Age: Managing Cybersecurity and Other Legal Risks with Connected Medical Devices
Device manufacturers: What legal and regulatory risks do you face with connected medical devices? What can you do to help mitigate the risks?
Join Scott Danzis, Jennifer Martin and Mark Young — all lawyers with Covington & Burling — on Aug. 10 as they delve into the FDA’s expectations related to cybersecurity.
After attending this webinar you’ll understand:
Register today and learn how to protect your company and patients from the risks of cyberattacks.
Meet Your Presenters
Scott Danzis, Partner, Covington & Burling, Food & Drug and Health Care
Scott Danzis’s practice focuses primarily on the regulation of medical devices, but also includes regulation of drugs, biologics, and tobacco products. He regularly works with companies in developing strategies for interacting with the FDA, including strategies for clinical development and premarket review.
Jennifer Martin, Counsel, Covington & Burling
Jennifer Martin has worked at the intersection of law and cybersecurity for the past 15 years. Her expertise in this area has been uniquely honed through her experience managing cyber risks and responding to threats from a variety of perspectives.
Mark Young, Special Counsel, Covington & Burling
Mark Young advises clients on data protection, cybersecurity and intellectual property matters. He has particular expertise in regulatory compliance, legislative advocacy and online IP enforcement.
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