Supplier Management for Medical Device Manufacturers

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

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

The Supplier Management for Medical Device Manufacturers brings together attendees from:

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

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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