Supplier Management for Medical Device Manufacturers 2019

  • 2019

Description

Supplier Management for Medical Device Manufacturers 2019 is a seminar that covers topics such as:

  • Creating a Risk-based Multi-tier supplier classification system
  • Understand FDA QSR and ISO 13485 requirements for supplier management
  • Defining and using supplier Metrics
  • Understand when suppliers have to register and list with the FDA
  • Develop an risk-based supplier management process
  • Explain the link between design control and purchasing data
  • Understand the how to develop and implement supplier controls
  • Create supplier measurement and monitoring systems
  • How to prepare yourself and your contract manufacturer for unannounced audits from your Notified body
  • Create a risk based Value-added system for supplier audits
  • Creating acceptance criteria and understand how that fits into your supplier control process

Supplier Management for Medical Device Manufacturers 2019 brings together:

  • Quality Engineers
  • Quality Managers
  • Supplier Engineers
  • Audit Managers
  • Supplier auditors
  • Internal quality auditors
  • Quality Specialists
  • Quality associates
  • Regulatory Compliance Managers

Past Events

Important

Please, check "Supplier Management for Medical Device Manufacturers" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Innovations, Quality assurance
Health & Medicine: Medical device, Medical technology

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