Effectively application of FMEA as a Risk Management Tool and meet ISO 13485:2003 Risk Management (ISO 14971) Requirements

Instructor: Angelo Scangas
Product ID: 700329
Training Level: Advanced
  • Duration: 60 Min

recorded version

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Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Mar-2007

Training CD / USB Drive

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In this Medical device training understand the expectations of FDA and the EU in applying risk analysis to medical devices.


Risk Management is required by ISO 13485 and risk analysis by the FDA’s Quality System Regulations (QSR) and by of the EU medical device regulations. Using practical examples, this course look at the regulatory and reporting requirements of EN ISO 14971, "Medical devices - application of risk management to medical devices".

The FMEA tool is used to provide an understanding of risk management and risk analysis techniques and methodologies, and to develop the skills required to apply these methodologies appropriate to a particular product. Risk management and analysis is considered throughout the entire life-cycle of the product, in design, production and distribution processes. The use of FMEA (Failure Mode and Effects Analysis) in identifying hazards, their severity, the probability that they might occur and the probability of preventing/detecting the hazard. are considered. Control measures and the monitoring of the effectiveness of such controls are discussed.

Areas Covered in the seminar:

  • Understand the expectations of FDA and the EU in applying risk analysis to medical devices
  • Understand the application of the risk analysis standard ISO 14971 to medical devices
  • Understand the application of risk analysis methodologies such as FMEA and FTA to medical devices
  • Understand the principles of risk management planning in developing procedures and practices to analyze, evaluate and control risks
  • Learn how to use a product safety audit to identify potential areas of risk exposure and liability exposure

Who Will Benefit:

  • R&D Managers / Engineers
  • Members of Design Review Teams
  • RA / QA Managers / Engineers
  • Sales and Marketing Management
  • Management Representatives
  • Product, Project, and Program Managers
  • Internal Auditors
  • Members of multi-discipline Design Teams

Instructor Profile:

Angelo Scangas, specializes in teaching process improvement, Lean Six Sigma, and various ISO certifications. You’ll benefit from Angelo’s extensive training experience in internal auditing, advanced product quality planning, FMEA, problem solving, project management, and SPC.

Angelo is a member of the ASQ Quality Management and Automotive Divisions, as well as AIAG, serving as a Certified AIAG, IAOB and RAB-Lead Auditor.

Follow us :
Critical Vendor Risk Management
Medical Device Summit 2018

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. ComplianceOnline 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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