Notified bodies and the FDA cannot require your suppliers to meet the quality system regulations, so they must make sure you are exercising sufficient control over those suppliers. You must make sure your supplier management and system meet all required regulations, especially for critical suppliers.
This class will review the QSR and ISO requirements for supplier evaluation, including defining the types of suppliers that require evaluation, including “critical” suppliers and outsourced processes. The QSR and ISO requirements for supplier assessment will be defined as well. The webinar will discuss the application of a risk-based process resulting in a customized supplier management system.
- Understanding of QSR requirements for supplier evaluation, and their application
- Understanding of ISO requirements for supplier evaluation, and their application
- Definition of types of suppliers, and those that require evaluation
- Best practices for “critical” suppliers and outsourced processes
- Understanding of QSR requirements for supplier assessment, and their application
- Understanding of ISO requirements for supplier assessment, and their application
- Application of risk-based process resulting in a customized supplier management system
- Review of FDA and ISO requirements
- Types of suppliers that must be qualified
- Defining critical suppliers
- Classification of suppliers
- Outsourced processes
- The Quality Agreement
- Recommended Practices
Supplier Assessment
- Review of FDA and ISO requirements
- Recommended Practices
- How to avoid “Death by Supplier Audit”
- Documentation requirements
- Supply chain management
- Buyers
- Purchasing management
- CAPA Coordinators
- Regulatory management
- QA management
- Executive management
- Internal auditors
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