ComplianceOnline

Effective DOE Strategies to Streamline your Processes for FDA Regulated Environment

Instructor: Jose Mora
Product ID: 700165
Training Level: Advanced
  • Duration: 60 Min

recorded version

$249.00
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

$500.00
One CD is for usage in one location only.
(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-963-2556

Email: customercare@complianceonline.com

Read Frequently Asked Questions

This DOE (Design of experiments) training focuses on DOE strategies. It is not focused on statistical methods, analysis of variance, and other techniques, but rather the overall approach for successful DOEs.

By the effective and progressive use of a Screening DOE, a Mapping DOE and a Robust Process DOE will lead to a better understanding of the process and the location of the best optimum. NOTE: This webinar focuses on DOE strategies. It is not focused on statistical methods, analysis of variance, and other techniques, but rather the overall approach for successful DOEs.

Areas Covered in the Session:

  • Gauge R&R considerations.
  • Screening DOEs
  • Mapping DOEs
  • Robust Process DOEs
  • Use of Six Sigma DMAIC when using DOEs and vice versa
  • Obtaining proper input from various stakeholders
  • Use of DOEs during process validation

What will Attendees Learn:

  • Effective DOE strategies
  • Avoiding pitfalls when performing DOEs
  • How to capture the essence of a process
  • Using the right resolution at the right time
  • Use of DOEs during process validation
  • How to prevent "expert" bias when designing experiments.
  • Letting the process do the talking.
  • "Poke the Alligator" - see how the process reacts

Who Will Benefit:

  • Manufacturing Engineers
  • Quality Engineers
  • Process Development Engineers and Scientists

Instructor Profile:

Jose Mora, is a Sr. Consultant at Streale as well as a partner in Atzari Consulting, LLC. Although he has been in the medical device industry for 24+ years in various companies, he has observed that the same types of issues and principles apply in all cases. Jose has worked as a Director of Manufacturing, Director of Manufacturing Engineering, Sr. Manufacturing Engineer, and as a Quality Systems Manager at companies such as V. Mueller (Cardinal Health), Cordis Corporation (J&J), Mentor Corporation, UroSurge (a startup urology products company), Boston Scientific, as well as several consulting clients. Jose has a BS. in Mechanical Technology from Purdue University.

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