ISO 13485, ISO 14971, Quality Document Management, and Risk Management for Medical Devices 2017

  • 21-22 Sep 2017
  • Quay West Suites Sydney Hotel, Australia

Description

ISO 13485, ISO 14971, Quality Document Management, and Risk Management for Medical Devices 2017 is a seminar that covers topics such as:

  • Inputs into a Quality and Regulatory Management System
  • Understand and implement a document naming convention for their department, pursuant to sections in ISO 13485
  • Incorporate the approach as a new discipline for all current and new staff joining the organisation
  • Procedural approach when documents are saved and are continuously traceable from the time they are first created
  • Immediate time savings when the approach is continuously used
  • Continuous use of the new procedure through ongoing audits of the practice throughout the organisation
  • Remain compliant to ISO 13485
  • A clearly defined document indexed maintainable folder structure

ISO 13485, ISO 14971, Quality Document Management, and Risk Management for Medical Devices 2017 brings together:

  • Quality professionals
  • Senior quality managers
  • Compliance professionals
  • Regulatory professionals
  • Manufacturing engineers
  • Production supervisors
  • Design engineers
  • Production engineers
  • Quality engineers
  • Process owners
  • Document control specialists
  • Quality auditors
  • IT Managers and associated staff
  • Administrative staff

Past Events

Important

Please, check "ISO 13485, ISO 14971, Quality Document Management, and Risk Management for Medical Devices" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Internal Audit & Compliance
Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Medical laboratories, Medical technology

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