An Overview of Risk Management and Risk Analysis Techniques

Instructor: Robert DiNitto
Product ID: 700206
Training Level: Basic
  • 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

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Read Frequently Asked Questions

In this Risk management training we will review the concept of Risk Management, its various elements, what is required, and its benefits.


How are you meeting the FDA and ISO risk management requirements? Hazard Analysis? FMECA? dFMEA/pFMEA? The concept of Risk Management and the difference between risk analysis, evaluation, assessment, and management.

The various forms of risk analysis will be described, highlighting their key characteristics and objectives as well as their differences. The relationship between risk analysis methods and which ones should be used will also be covered. We will discuss examples of some of the most commonly used forms of risk analysis, explaining the techniques and terminology used, and will review who should perform them and when they should be performed. We will also discuss the evaluation and acceptability of overall residual risk. We will also review the Risk Management Plan, the Risk Management Report, and the Risk Management File.

Areas Covered in the Seminar:

  • Risk analysis, risk evaluation, risk assessment, and risk management
  • The benefits of risk analysis and risk management
  • Description of the different risk analysis methods
  • Qualitative vs quantitative risk analysis
  • Hazard Analysis
  • dFMEA & pFMEA
  • Fault Tree Analysis
  • Comparison of risk analysis methods: their relationships and differences
  • Residual Risk
  • Risk acceptability
  • Risk management planning

Who Will Benefit:

  • Quality Assurance managers and personnel
  • R&D managers & engineers
  • Regulatory Affairs personnel
  • Quality system auditors

Instructor Profile:

Robert DiNitto is a principal and one of the founders of AlvaMed, LLC, an innovative medical technology consulting firm. He leads AlvaMed’s QA/RA and Design Control practice, having over 35 years of experience in the medical device industry. Bob has developed and implemented design control systems that have been well received by both engineering organizations and regulatory auditors, and received a high approval rating from an FDA auditor. His engineering experience, in roles ranging from project engineer to VP of R&D, covers many types of products from small, portable monitors with sterile disposables to large x-ray systems. He has designed electrical and mechanical hardware and software. Bob has assisted numerous companies with development planning, including providing training and document templates for development, V&V, manufacturing, risk management, and regulatory plans as well as conducting hazard analyses and FMEAs, developing appropriate, easy-to-use risk rating scales and training personnel on risk analysis basics.

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Seminars by Ex-FDA Officials
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.

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Product Reviews Write review

This webinar was very informative.
- Anonymous

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