Medical Device Cybersecurity -Improving Compliance and your Company's Bottom Line


Tuesday, September 11, 2018   |   10:00 AM PDT | 01:00 PM EDT   |   Duration: 90 Minutes      

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Duration: 90 Minutes  

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This webinar will identify the FDA's fundamental premarket and postmarket requirements that involve software.
Carolyn Troiano   Product Id : 502077
  Instructor : Carolyn Troiano

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Overview:

This session will provide some insight into current trends in cybersecurity threats to medical devices and how to follow industry best practices to prevent and/or mitigate these threats. Cybersecurity is a serious concern for medical device safety and effectiveness. Without protection, software running on a medical device could cause severe injury or death to a patient.

There are many forms of cybersecurity and many remedies for thwarting attempts to penetrate medical device software. Most of these are based in physical and logical security practices that are becoming best industry practices. This webinar will detail some of the threats and ways to mitigate them to protect consumers from harm.

Why should you Attend: Providing safe and effective medical devices is in the best interests of all those involved in the development, manufacturing, testing, and distribution of these products. One of the largest current threats to these devices working safely and effectively is cyberattacks that can wreak havoc on code and device functionality. Preventing these attacks by identifying sources of threats and rooting them out before they can take effect is of the utmost concern.

In this webinar, you will learn just how cyberattacks threaten medical devices and how industry is currently responding to them. We will discuss the many ways of preventing and mitigating the cybersecurity risk, and about the industry best practices that can help your company do the same. data.

Areas Covered in the Session:

  • Provide an overview of cybersecurity and guidance on device software
  • Provide an overview of the most common problems faced by industry in terms of medical device security, efficacy, and safety
  • Provide a set of best practices and industry standards to meet the challenges of cybersecurity and other threats to devices and software

Who Will Benefit:
  • Medical Device Manufacturing
  • Testing
  • Packaging and Distribution companies


Speaker Profile
Carolyn (McKillop) Troiano has more than 35 years of experience in the tobacco, pharmaceutical, medical device and other FDA-regulated industries. She has worked directly, or on a consulting basis, for many of the larger pharmaceutical and tobacco companies in the US and Europe, developing and executing compliance strategies and programs. Carolyn is currently active in the Association of Information Technology Professionals (AITP), and Project Management Institute (PMI) chapters in the Richmond, VA area.

During her career, Carolyn worked directly, or on a consulting basis, for many of the larger pharmaceutical companies in the US and Europe. She developed validation programs and strategies back in the mid-1980s, when the first FDA guidebook was published on the subject, and collaborated with FDA and other industry representatives on 21 CFR Part 11, the FDA’s electronic record/electronic signature regulation.




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