Medical Device Cybersecurity Following Latest FDA Guidance

Posted By : User Ref No: WURUR52765 0
  • Image
  • TypeWebinar
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  • Location Fremont, California, United States
  • Price
  • Date 10-03-2020
Medical Device Cybersecurity Following Latest FDA Guidance, Fremont, California, United States
Webinar Title
Medical Device Cybersecurity Following Latest FDA Guidance
Event Type
Webinar
Webinar Date
10-03-2020
Last Date for Applying
09-03-2020
Location
Fremont, California, United States
Organization Name / Organize By
Compliance4all
Organizing/Related Departments
Online Training
Organization Type
Organization/Company
WebinarCategory
Both (Technical & Non Technical)
WebinarLevel
All (State/Province/Region, National & International)
Related Industries

Education/Teaching/Training/Development

Engineering

Business Development

Manufacturing

Medical/Healthcare/Hospital

Location
Fremont, California, United States

Overview:

The company must establish a program where they identify, analyze and control cybersecurity risks for both pre market and post market. The cybersecurity program must be carefully planned.

A formal special hazard analysis must be conducted for each risk. Communication of risks must be sent to device users. A complex set of reporting requirements has been established. This webinar will describe a program that will be compliant to the FDA requirements

Why you should Attend:Medical device cybersecurity has become very important to the FDA. They have recently issued two Guidance’s on the subject; the latest in December of 2016. FDA expects a proactive extensive risk-based program to minimize risk to the user from cyber-attacks including active involvement with information sharing groups

Areas Covered in the Session:

  • Cybersecurity Plan
  • Risk-based Analysis
  • Hazard Analysis following ISO14971
  • Risk Communication to users
  • Required Membership in information sharing groups
  • Reporting Requirements and Exceptions


Who Will Benefit:

  • Company Management
  • IT Personnel
  • Development Engineers
  • Production Management
  • QA/ QC Personnel
  • Software Developers
  • Cybersecurity, ISAO, risk

 

 

Speaker Profile

Edwin Waldbusser is a consultant retired from industry after 20 years in management of development of medical devices (5 patents). He has been consulting in the US and internationally in the areas of design control, risk analysis and software validation for the past 8 years. Mr. Waldbusser has a BS in Mechanical Engineering and an MBA. He is a Lloyds of London certified ISO 9000 Lead Auditor and a member of the Thomson Reuters Expert Witness network.

 

Event link:

https://www.compliance4all.com/webinar/--502939LIVE?channel=eventsget_2020_SEO

Contact Info

Netzealous LLC, DBA -Compliance4all

Email: [email protected]

Phone: +1-800-447-9407

Website: https://www.compliance4all.com/

Others Details

Contact Info Netzealous LLC, DBA -Compliance4all Email: [email protected] Phone: +1-800-447-9407 Website: https://www.compliance4all.com/

Registration Fees
Available
Registration Fees Details
$150
Registration Ways
Website
Address/Venue
  Online  Pin/Zip Code : 94539
Landmark
California
Official Email ID
Contact
Netzealous LLC,DBA -Compliance4all

Online

[email protected]

   8004479407    Fax No: 94539