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Shannon Lantzy MedCrypt New VP of Consulting

Lantzy Will Leverage Her Regulatory Science & Business Transformation Experience fron Working with Booz Allen Hamilton, the FDA, & NASA to Launch MedCrypt's Consulting Services

MedCrypt the proactive cybersecurity solution provider for medical devices, today announced the addition of Shannon Lantzy, Ph.D., as their new Vice President of Consulting.

Prior to joining MedCrypt, Shannon Lantzy spent six years with Booz Allen Hamilton where she led the Regulatory Science Innovation team, partnering with the U.S. Food and Drug Administration (FDA) to develop, test, and evaluate new approaches to regulatory decisions and benefit-risk assessments.

Shannon Lantzy also co-founded Booz Allen’s Secure Connected Health practice and brought together a diverse set of experts, cybersecurity tools, and strategies to solve cybersecurity challenges relating to patient safety. Before Booz Allen, Lantzy was a consultant for NASA, helping with organizational strategy, capability assessment, enterprise architecture, technology adoption, and process improvement. Lantzy earned a Ph.D. in Information Systems from Robert H. Smith School of Business at the University of Maryland.

“Advancements in connected technology have paved the way for a future of healthcare that is digital and delivered in new environments,” said Shannon Lantzy, MedCrypt Vice President of Consulting. “To build this digital landscape and to support future innovation, healthcare needs a baseline of secure infrastructure. The MedCrypt team is working with some of the world’s largest medical device manufacturers to improve their medical device security posture and I am both eager and proud to join in on their efforts.”

At MedCrypt, Shannon Lantzy will be responsible for leading MedCrypt’s Consulting Services to bring clinically innovative medical devices that are secure by design through their lifecycle. She will lead and support consulting engagements, ensuring MedCrypt’s customers meet their business outcomes and the pre-and post-market cybersecurity guidelines from the FDA.

“I met Shannon at a healthcare-related event several years ago and was immediately impressed with her passion and drive to move healthcare into a digital future,” said Mike Kijewski, CEO of MedCrypt. “We’re excited to have Shannon join our team to help our customers transform from reactive to proactive product security.”

Other Executives In the News

SourceMedCrypt
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Medical Device News Magazine provides breaking medical device / biotechnology news. Our subscribers include medical specialists, device industry executives, investors, and other allied health professionals, as well as patients who are interested in researching various medical devices. We hope you find value in our easy-to-read publication and its overall objectives! Medical Device News Magazine is a division of PTM Healthcare Marketing, Inc. Pauline T. Mayer is the managing editor.

Executives on the Move

Dr A Burton Tripathi brings over two decades of Medical Device leadership experience, specializing in developing disruptive technologies, leading commercialization efforts, and facilitating M&A. Having recently served as CEO of TrueVision Systems Inc., he concluded the sale and integration of TrueVision with Alcon.
John Taylor brings more than 30 years of regulatory experience to his role at ELIQUENT, including a distinguished 20-year career at the U.S. Food and Drug Administration (FDA), where he served in multiple leadership positions, including as FDA’s Acting Deputy Principal Commissioner, FDA Counselor to the Commissioner, Acting Deputy Commissioner for Global Regulatory Operations and Policy, and Associate Commissioner for Regulatory Affairs.
Jennifer Riter comes to Kindeva from West Pharmaceutical where she spent the past 27 years in various technical and leadership roles, most recently serving as the Senior Director, Business and Technical Operations.

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