Creation and management of a Controlled Document System for a Life Sciences manufacturing plant util (Controlled documents)

Venue: Online Training Webinars

Location: Wilmington, Delaware, United States

Event Date/Time: Aug 09, 2011 End Date/Time: Aug 09, 2011
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Description

Overview: Controlled documents are one of the foundational building blocks of a Quality Management System (QMS) for regulated industries.

Too often, controlled documents are cluttered, confusing, and cause many errors due to the way they are created, organized, and managed. This webinar applies the Theory of Lean Documents and the corresponding Theory of Lean Configuration to this key part of a QMS.

Why you should attend: Do you find yourself constantly struggling to create, manage, and maintain all of the information found in controlled documents - 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 documentation and not enough on engineering, quality, and operations? This webinar presents a fresh new approach based upon solid principles and proven practices - as well as an alternative that avoids many of the pitfalls of traditional ways of preparing these documents.

Areas Covered In the Session:

Brief introduction to Lean Documents and Lean Configuration
Quality System Regulation, 21 CFR Part 820, and ISO 13485 as these apply to controlled documents.
Typical controlled documents and functions
Lean principles applied to controlled documents
Lean principles applied to configuration of electronic QMS software

Who will benefit:

Managers, Supervisors, Directors, and Vice-Presidents in the areas of:
R&D
Manufacturing Engineering
Quality Assurance
Operations
Document Control

Price List:
Live : $245.00
Corporate live : $995.00
Recorded : $295.00

Venue

1000 N West Street | Suite 1200
Wilmington
Delaware
United States
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