This training on lean documents and document control will explain the different types of documents and the usage of lean document principles. Attendees will also learn types of controlled documents; examples of lean and non-lean controlled documents, pros and cons of lean vs. non-lean documents.
Why Should You Attend:
Just as a manufacturing process produces a product, controlled documents are the product of a business process. Just as in manufacturing, a product cannot move forward if it is waiting for component parts, a document cannot move forward if it is waiting for information, or if its use is constrained by other documents.
Who Will Benefit:
This webinar will provide valuable insights to:
Design engineers
Manufacturing engineers
Operations managers
Quality system managers
Document control managers
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 NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2016.
For Registration:
http://www.complianceonline.com/lean-documents-and-document-control-fda-requirements-webinar-training-701653-prdw?channel=sciencedz