LEARN HOW TO APPLY THE PRINCIPLES OF LEAN DOCUMENT 2015 - 21 CFR Part 820 Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration

Website http://bit.ly/1E2jwg7 | Edit Freely

Category FDA Compliance;

Deadline: March 11, 2015 | Date: March 11, 2015

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

Updated: 2015-03-10 16:43:36 (GMT+9)

Call For Papers - CFP

Why Should you Attend:

If you are constantly struggling to create, manage, and maintain all of the information found in controlled documents, all of which are often redundant, repetitive, and clustered together in an awkward manner, this webinar is something that will give you a different perspective and a very different approach that you can use.

Who Will Benefit:

This webinar will provide valuable assistance to Managers, Supervisors, Directors, and Vice-Presidents in the areas of:

R&D

Manufacturing Engineering

Design Assurance

Quality Assurance

Operations

Instructor Profile:

Jose 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, Jose 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/21-cfr-part-820-quality-system-regulation-compliant-lean-documents-webinar-training-703300-prdw?channel=ourglocal