This on demand webinar will cover the following topics:
- Regulatory requirements for supplier qualification
- Responsibilities of manufactures and suppliers
- Best practices for supplier selection, qualification, and management
- What are the FDA's expectations in regards to Quality Agreements?
- What is meant by the title owner, contractor, adulterated drug, and the term manufacturing within the guidance?
- Best practices for a good quality agreement
- Supplier audits
- Documentation requirements and audit trials
