Corrective Actions - Current Expectation of ISO 13485 and FDA Auditors 2015

  • 27 Aug 2015
  • Webinar

Description

Corrective Actions - Current Expectation of ISO 13485 and FDA Auditors 2015 is a webinar that covers topics such as:

  • Why Containment and Correction have been overlooked
  • Overview of CAPA system for Current ISO 13485 compliance
  • What is really the difference between correction and corrective action
  • Why this is a hot item with ISO auditors
  • Defining and documenting Containment actions - Quickly
  • What kinds of containment can be done for Quality System nonconformities
  • Examples of Containment actions
  • Where does Preventive Action fit in

Corrective Actions - Current Expectation of ISO 13485 and FDA Auditors 2015 is intended for:

  • QA Specialists
  • Quality Managers
  • Quality Engineers
  • CAPA coordinators
  • Operations managers
  • Engineers doing Corrective Actions
  • Quality auditors
  • Manufacturing Engineers
  • Medical device Consultants

Past Events

Important

Please, check "Corrective Actions - Current Expectation of ISO 13485 and FDA Auditors" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Quality assurance
Education: E-learning, Training
Government & Global Issues: Law & Regulations
Health & Medicine: Medical laboratories, Medical technology
Science: Education Sciences, Health sciences

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