Using Risk Analysis to Optimize Product Development and Manufacturing

Instructor: Robert DiNitto
Product ID: 700166
Training Level: Intermediate
  • Duration: 60 Min

recorded version

1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section

Training CD / USB Drive

One CD/USB is for usage in one location only.
(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-362-2367


Read Frequently Asked Questions

This Risk Analysis training guide you through the methodologies of and distinctions between Hazard Analyses, dFMEAs, and pFMEAs and step beyond performing Risk Analyses and documenting mitigations to the practical and proactive application.


Did you know that you can use your existing Risk Analyses to help you do more than manage risk? Risk Analyses can be used to prioritize and streamline Design Input, Design Output, Design V&V, and both Pre-Production.

Focusing on the wrong product development or manufacturing activities can not only waste your time and money but can affect the quality of your product and leave you unprepared for regulatory audits.

In this presentation, we will show you

  • How to target your Design Input activities to focus on those areas that improve safety, minimize risk and improve quality
  • How Design Output feeds back to Design Input using the Risk Analysis process
  • How to target your Design V&V and Process Validation plans to the most critical aspects of your product and determine the minimum number of samples needed
  • How to reduce or eliminate testing and inspections that do not bring value to your product or your business

An adequate testing, inspection and sampling plan will save you time and money while also helping you deliver safer, higher quality products to your customers.

This webinar - which assumes a basic understanding of the methodologies of and distinctions between Hazard Analyses, dFMEAs, and pFMEAs - will take you a step beyond performing Risk Analyses and documenting mitigations to the practical and proactive application of Risk Analysis results to achieve additional benefits.

Areas Covered in the seminar:

  • How to use the HA to drive Design Input Requirements
  • How to use the dFMEA as an additional link from Design Output back to Design Input
  • How to use Risk Analysis as a tool in formulating your Design V&V strategy, including how to develop a risk based sampling plan
  • How to use Risk Analysis as a tool in formulating your Process Validation strategy
  • How to use the results of your Process Validation Strategy to drive your Inspection and Test Strategy
  • How to safely reduce testing and inspections done in Production without compromising quality

Who Will Benefit:

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

Instructor Profile:

Bob 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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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.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email call +1-888-717-2436 (Toll Free).

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