21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration 2017
28 Feb 2017
Webinar
Description
Topics
Quality System Regulation, 21 CFR Part 820, and ISO 13485 as these apply to design control documents
Brief introduction to lean documents and lean configuration
Key types of controlled documents and records for manufacturing
Basic functions found in a life sciences manufacturing plant
Bringing it all together
Quality Management System (QMS) elements controlled via documentation
Who should Attend
Senior attendees with responsibilities in:
Manufacturing Engineering
R&D
Quality Assurance
Design Assurance
Document Control
Operations
Past Events
21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration 2017 - 28 Feb 2017, Webinar (65727)
Important
Please, check "21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Medical device, Medical technology, Pharma
