Supplier Management for Medical Device Manufacturers 2016 is a conference that covers topics such as:
- FDA`s multitier supplier classification system
- Understand FDA QSR, ISO 13485:2003, and ISO 13485:2016 requirements for supplier management
- Analysis matrix and radar chart to compare suppliers
- When suppliers have to register and list with the FDA
- An overall supplier management plan
- The link between design control and purchasing data
- Create receiving inspection criteria and use them as part of supplier controls
- How to develop and implement supplier controls
- The three application of risk management: business risk, regulatory risk, and medical device risk
- Develop supplier measurement and monitoring systems
- Developing a supplier audit using the backward trace process approach
- How to determine when to audit a supplier and the audit`s scope
Supplier Management for Medical Device Manufacturers 2016 brings together attendees from:
- Supply Chain Managers
- Quality Managers
- Supplier Quality Engineers
- Quality Engineers
- Regulatory Specialists
- Purchasing Professionals
- Design and Development Engineers
- Production and Process Engineers
- Verification and Validation Specialists