The Supplier Management for Medical Device Manufacturers 2016 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 2016 brings together attendees from:
- Quality Engineers
- Quality Managers
- Supplier Engineers
- Audit Managers
- Supplier auditors
- Internal quality auditors
- Quality Specialists
- Quality associates
- Regulatory Compliance Managers
