21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Configuration 2015

  • 28 Jul 2015
  • 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
  • Quality Management System (QMS) elements controlled via documentation
Who should Attend

Supervisors, Managers, Vice-Presidents and Directors in the areas of:

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

Past Events

Important

Please, check "21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Configuration" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Innovations, Internal Audit & Compliance, Operations, Quality assurance
Health & Medicine: Pharma
Science: Life Sciences & Biology
Technology: Biotechnology

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