DMR & DHR - What Is Really Required 2012

  • 29 Feb 2012
  • Webinar

Description

Topics
  • Key Definitions
  • The FDA’s QSR
  • Quality System Record (QSR)
  • Design History File (DHF)
  • Device History Record (DHR)
  • Device Master Record (DMR)
Who should Attend

People involved in design, project management, purchasing, production, servicing, installation, record keeping activities and document control for medical device manufacturing including: Quality Professionals, Quality Managers, Production Managers, Regulatory Professionals, Project Managers, Risk Managers, Manufacturing Engineers, Production Supervisors, Design Engineers, Production Engineers, Quality Engineers, Process Owners, Document Control Specialists, Quality Auditors and Record Retention Specialists.

Past Events

Important

Please, check "DMR & DHR - What Is Really Required" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical device

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