Quality Audits for the Medical Device Industry 2017

  • 02-03 Mar 2017
  • San Diego, CA, United States

Description

The Quality Audits for the Medical Device Industry 2017 is a workshop that covers topics such as:

  • The difference among audit methods (system, product, process, etc.)
  • Learn the difference among the audit types
  • The role of auditor competency and how to determine it
  • Audit scheduling and methods to establish and update the schedule
  • The role of correction and corrective action related to an audit nonconformance
  • Which audits an auditor could conduct and which ones to avoid
  • Develop an effective approach for reporting at management review

The Quality Audits for the Medical Device Industry 2017 brings together attendees from:

  • Lead Auditors
  • Audit Managers
  • Management Representative
  • Audit Team Members
  • Quality Engineers
  • Quality Assurance Managers
  • Supplier Management and Purchasing
  • Regulatory Affairs Managers
  • Supplier Quality Engineers

Past Events

Important

Please, check "Quality Audits for the Medical Device Industry" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Facility planning & Management, Finance, Internal Audit & Compliance, Management, Quality assurance
Health & Medicine: Hospitals & Clinics, Medical device, Medical laboratories, Medical technology
Technology: Information Technology (IT)

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