FDA`s Expectations from Supplier Management for GMP: Quality Agreements and More 2019 is a webinar that covers topics such as:
- Responsibilities of manufactures and suppliers
- Regulatory requirements for supplier qualification
- What are the FDA’s expectations in regards to quality agreements?
- Best practices for supplier selection, qualification and management
- Best practices for a good quality agreement
- What is meant by the title owner, contractor, adulterated drug, and the term manufacturing within the guidance?
- Documentation requirements and audit trails
- Supplier audits
FDA`s Expectations from Supplier Management for GMP: Quality Agreements and More 2019 is intended for:
- Regulatory Affairs/Regulatory Compliance Directors, Managers, and Specialists
- Quality Assurance/Quality Control Directors, Managers, and Specialists
- Engineering/Development Directors, Managers, and Specialists
- Purchasing/Materials Management Directors, Managers, and Specialists
- Document Control Managers and Specialists
