ComplianceOnline

Best Practices on Six Sigma and CAPA Convergence

Instructor: Jose Mora
Product ID: 700168
Training Level: Intermediate
  • 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 Quality compliance training will helps in methodologies of Six Sigma and CAPA converging and how to recognize which methodology is best to use for a problem.

Simply documenting "it broke - I fixed it" does very little to instill permanent solutions. Six Sigma methodology is an ideal toolbox for drilling into the root causes of problems and making certain that permanent solutions are in place. The true spirit of CAPA and Six Sigma is the improvement fo the overall system and the reduction in variation around a previously established "centered" process. Too many companies focus on the speed with which CAPAs are closed, yet pay too little attention to the effectiveness and longevity of the solution.

Areas Covered in the Session:

  • Why are the methodologies of Six Sigma and CAPA converging?
  • How to recognize which methodology is best to use for a problem.
  • How should my quality systems work together?
  • Best Practices
  • Should Electronic Signatures apply to my Enterprise Six Sigma system?

Who Will Benefit:

  • Quality System Managers
  • Operation Managers
  • Engineering Managers
  • Other similar quality, operations
  • and engineering personnel

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
Recordkeeping and Documentation in a GLP Laboratory

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