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2017 - Root Cause Analysis for CAPA & Best Practices - 2017

Date2017-12-12

Deadline2017-12-11

VenueFremont, USA - United States USA - United States

KeywordsCompliance Specialists; Manufacturing Engineers; CAPA Managers

Websitehttp://www.compliance4all.com/control/w_...

Topics/Call fo Papers

Overview:
Refund Policy
By attending this webinar you will learn about the RCA toolbox and how to get permanent resolution to your significant quality problems.
Why should you Attend:
You will waste precious time and money and still end up with unsatisfactory results. This webinar will give you insights and lessons learned from a certified Master Black Belt and industry expert with over 30 years' experience.
Areas Covered in the Session:
Build the right team
Develop a problem statement
Failure Investigation
Data Collection
Who Will Benefit:
Quality Engineers
Manufacturing Engineers
Process Engineers
Compliance Specialists
Auditors
Speaker Profile:
Susanne Manz MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma. She has an extensive background in quality and compliance for medical devices from new product development, to operations, to post-market activities.
Event Fee: One Dial-in One Attendee Price: US$150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support-AT-compliance4All.com

Last modified: 2017-10-26 14:45:59