21 CFR Part 820 2017 - Applying Principles of Lean Documents and Lean Configuration

Overview:
In this webinar, we apply the Theory of Lean documents and its corollary
Theory of Lean Configuration to present a fresh approach to following 21
CFR Part 820.
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.
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 design control documents
Basic functions found in a life sciences manufacturing plant
Key types of controlled documents and records for manufacturing
Quality Management System (QMS) elements controlled via
documentation
Bringing it all together
Who Will Benefit:
Managers, Supervisors, Directors, and Vice-Presidents
R&D
Manufacturing Engineering
Design Assurance
Quality Assurance
Operations
Document Control
Speaker 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 industry specializing in manufacturing, process
development, tooling, and quality systems. Prior to working full time as a
consulting partner for Atzari Consulting, José 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.
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support-AT-compliance4All.com