Design History File (DHF) Device Master Record (DMR) Device History Record (DHR) and Technical File (TF) - Regulatory Documents Explained 2011

  • 25 Aug 2011
  • Webinar

Description

Design History File (DHF) Device Master Record (DMR) Device History Record (DHR) and Technical File (TF) - Regulatory Documents Explained is a webinar that covers topics such as:

  • Design History File (DHF)
  • MDD Requirements/Definitions
  • Device History Record (DHR)
  • Device Master Record (DMR)
  • Design/process changes and DHF, DMR, DHR, and TF
  • Technical File (TF)

Design History File (DHF) Device Master Record (DMR) Device History Record (DHR) and Technical File (TF) - Regulatory Documents Explained brings together device manufacturers, who market within the US or wish to market in the EU including Production/Process Managers/Engineers, Quality Managers/Engineers, QA and QC managers, inspectors, supervisors and personnel, Manufacturing Managers/Engineers, Supplier Quality Managers/Engineers, Documentation Specialists and Regulatory Managers/Engineers.

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Important

Please, check "Design History File (DHF) Device Master Record (DMR) Device History Record (DHR) and Technical File (TF) - Regulatory Documents Explained" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Pharma

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