Establishing a Medical Device Security Program

In this medical devices security webinar you will learn how to establish a Product Security Program that help your organization to put the right people, processes, and technology in one place to solve the changing landscape of connected medical devices and the risks that are associated with the new environment. It will also highlight the medical device security leading best practices the industry has been implementing to not only meet regulatory requirements but also increasing customer’s needs.

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Areas Covered in the Webinar:
  • Medical device security risks / overview
  • Industry landscape
  • Product Security Program
  • What are leading practices?
  • Key takeaways
Who Will Benefit:
  • Medical device manufacturers (Product / Quality / IT / Security Teams)
  • Healthcare delivery organizations (IT / Biomedical Teams)
  • Patients / Concerned consumers
  • Security Professionals
Instructor Profile:
Robert Mai Robert Mai

Senior Manager, Cyber Risk Services at Deloitte and Touche LLP

Over 15 years of experience in information technology, security, regulatory compliance, and business process & technology controls. He has served his clients in a wide range of cyber risk roles which includes establishing and enhancing security, privacy, and compliance programs; cyber security strategies/roadmaps based on leading industry and regulatory requirements (HIPAA, NIST, ISO, PCI, SOX, FDA) etc.

Global portfolio leader for Deloitte's MeDSS practice. In this role, Robert assists medical device manufacturers and healthcare delivery organizations in designing, developing, and implementing holistic medical device security programs. He has led multiple initiatives with his client around medical device security program governance, maturity assessments, product security risk assessments, and technical security testing.

Lucas Rice Lucas Rice

Senior Consultant, Cyber Risk Services at Deloitte and Touche LLP

Lucas Rice is a Senior Consultant specializing in product security within Deloitte & Touche’s Cyber Risk practice. He is a member of Deloitte’s Medical Device Safety and Security (MeDSS) team, which helps product manufacturers manage the risks associated with their developed, marketed, and fielded products and customers manage the risks of their acquired products.

On the team, Lucas is the Process Solutions Lead, whose experience includes advising clients on product security process solutions through performing maturity assessments of product security programs, helping clients design, develop, implement, and operate product security programs, and providing clients with a roadmap for how to integrate security processes into their product development lifecycle.

Lucas has had the opportunity to serve a number of clients on the MeDSS team, ranging from large device manufacturers, to regional hospitals. He has also had experience helping a wide range of organization in other industries with their cyber security and product security programs: from technology and utilities to chemicals and heavy equipment organizations.

Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. FDATrainingAlert would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

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