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

  • 28 Feb 2017
  • Webinar

Description

@@ is a webinar that covers topics such as:

  • 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

21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration 2017 is intended for senior attendees with responsibilities in:

  • Manufacturing Engineering
  • R&D
  • Quality Assurance
  • Design Assurance
  • Document Control
  • Operations

Past Events

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
Science: Life Sciences & Biology

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