FDAnews Announces — Conducting a Connected Medical Device Security Risk Assessment Webinar, Oct. 25, 2016

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How can device manufacturers understand the cybersecurity and privacy risks related to getting approval for new products and their exposure to both fielded and legacy devices? Join security risk specialists Russell Jones and Nick Sikorski — both with Deloitte & Touche — on Oct. 25 when they’ll discuss how security risk assessments need to be conducted and how to develop remediations to reduce risks to an acceptable level.

Conducting a Connected Medical Device Security Risk Assessment
**An FDAnews Webinar**
Oct. 25, 2016 — 1:30 p.m. – 3:00 p.m. ET
http://info.fdanews.com/conducting-a-connected-md-security-risk-assessment-pr

What are the chances of a cybersecurity breach?

Medical devices are increasingly interconnected to the internet and hospital networks. An attack could affect how a device operates and endanger users.

How can device manufacturers understand the cybersecurity and privacy risks related to getting approval for new products and their exposure to both fielded and legacy devices?

Join security risk specialists Russell Jones and Nick Sikorski — both with Deloitte & Touche — on Oct. 25 when they’ll discuss how security risk assessments need to be conducted and how to develop remediations to reduce risks to an acceptable level.

By attending this 90-minute webinar manufacturers will learn:

  •     What threats have emerged as medical device functionality has grown
  •     The risks that are arising as a result of the fast changing cybersecurity landscape
  •     The impact of the FDA’s recently released draft guidance on 510(k) submissions related to the design, development, maintenance, and disposition on connected medical devices
  •     New and emerging standards and guidance for connected medical device cybersecurity (e.g. AAMI TIR57) and how they can be used to secure connected medical devices
  •     How to conduct a connected medical device security risk assessment aligned with industry leading practices
  •     Where the industry may be going next regarding cybersecurity of connected medical devices

Register today and hear about evolving leading practices for conducting security risk assessments on connected medical devices.

Meet the Presenters:
Russell L. Jones, Partner, Deloitte & Touche LLP, Life Sciences & Healthcare Sector – Cyber Risk Services:

Russell has more than 23 years of experience working with health care providers, biopharma/diagnostic companies, medical device manufacturers and public sector clients addressing a wide variety of information security, cybersecurity, data privacy and IT risk management problems.

Nick Sikorski, Senior Consultant, Deloitte & Touche LLP, Life Sciences & Healthcare Sector – Cyber Risk Services:

Nick is the Global Program and Solutions Leader for Deloitte & Touche’s Medical Internet of Things (Medical IoT) practice responsible for securing connected and networked medical devices and additional Life Sciences products developed by medical device manufacturers.

Who Will Benefit:

  •     QA/QC personnel
  •     Data management and statistics personnel
  •     Engineering and design controls teams
  •     Risk management specialists
  •     Compliance officers

Webinar Details:
Conducting a Connected Medical Device Security Risk Assessment
Oct. 25, 2016 — 1:30 p.m. – 3:00 p.m. ET
http://info.fdanews.com/conducting-a-connected-md-security-risk-assessment-pr

Tuition:
$287 per site

Easy Ways to Register:
Online:     http://info.fdanews.com/conducting-a-connected-md-security-risk-assessment-pr                            
By phone: 888-838-5578 or 703-538-7600

About FDAnews:
FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations.

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Michelle Butler
FDANEWS
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