Corrective and Preventive Action Utilizing the Principles of Lean Documents and Lean Configuration

Website http://bit.ly/19w23Vp | Edit Freely

Category FDA Compliance;

Deadline: April 03, 2015 | Date: April 03, 2015

Venue/Country: Palo Alto, U.S.A

Updated: 2015-03-31 20:04:52 (GMT+9)

Call For Papers - CFP

Why Should You Attend:

Do you find yourself constantly struggling to create, manage, and maintain all the information found in Corrective and Preventive Actions (CAPA) - which is often redundant, repetitive, and chained together in a cumbersome way?

Do you find that your design and manufacturing resources are spending way too much time on documenting the CAPA process and not enough time on actually correcting and preventing systemic issues?

Who Will Benefit:

R&D Staff

Manufacturing Engineering

Design Assurance

Quality Assurance

Operations

Instructor Profile:

José Mora is a principal consultant specializing in manufacturing engineering and quality systems. For over 30 years, he has worked in the medical device and life sciences industry specializing in manufacturing, process development, tooling, and quality systems. Prior to working full time as a consulting partner for Atzari Consulting, Mr. Mora served as director of manufacturing engineering at Boston Scientific and as quality systems manager at Stryker Orthopedics, where he introduced process performance, problem solving, and quality system methodologies.

Note:

Use coupon code 232082 and get 10% off on registration.

For Registration:

http://www.complianceonline.com/corrective-action-utilizing-the-principles-of-lean-documents-and-lean-configuration-webinar-training-703879-prdw?channel=ourglocal