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 / USB Drive

$500.00
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

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.

Follow us :
Upcoming In-person Seminars by EX-FDA OFFICIALS
PV (Pharmacovigilance) Audit Strategy Planning

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 customercare@complianceonline.com call +1-888-717-2436 (Toll Free).

Product Reviews

This product hasn't received any reviews yet. Be the first to review this product! Write review

Best Sellers
You Recently Viewed
    Loading