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