In this Medical device training will show you how to make the DFMEA process work for you. How to use the process to help focus your testing matrix to target the most critical aspects of the product's design and function.
This presentation will show you how to make the DFMEA process work for you, what value it has for each function in your organization (development, marketing, quality, etc.), and how to use the process to help focus your testing matrix to target the most critical aspects of the product's design and function, helping you deliver a higher quality design to your customers.
This presentation will show you how to make the DFMEA process work for you, what value it has for each function in your organization (development, marketing, quality, etc.), and how to use the process to help focus your testing matrix to target the most critical aspects of the product's design and function, helping you deliver a higher quality design to your customers.
Areas Covered in the seminar:
- Why FMEAs are required
- How to use a DFMEA/FMEA to help reduce risk
- The common mistakes in determining occurrence and severity rankings
- What you can and cannot affect to reduce your RPN (Risk Priority Number)
- Determining an RPN threshold
- Revising and updating your FMEAs
Who Will Benefit:
- Quality Assurance managers and personnel
- R&D managers & engineers
- Quality system auditors
Course Provider
Robert DiNitto,
