Risk-based Supplier Management System: ImpactImpact on Regulatory and Operational Goals for Medical Device Manufacturers 2015 covers topics such as:
- Learn about the two guidelines that cover current FDA and ISO 13485 expectations for supplier control
- Understand the types of suppliers that must be qualified according to the FDA and ISO 13485
- Understand how to create or bring your supplier program into compliance with the these guidance documents while optimizing the resources needed to comply
- Understand how to use the Global harmonization Task Forces (GHTF) and NBOC supplier guidance documents that you could be audited to
- Understand how to define and control supplier risk and why this benefits your company
- Understand requirements for Critical suppliers
- Learn about best practices for supplier qualification and control
Risk-based Supplier Management System: ImpactImpact on Regulatory and Operational Goals for Medical Device Manufacturers 2015 brings together attendees from:
- Regulatory Affairs
- Quality Management
- Supplier Engineering
- Supply-Chain Management
- Supplier Auditing
- Purchasing Management
- Quality Engineering
- Internal Auditing