This webinar will provide insights on building sustainable vendor qualification program specific to the FDA regulated industries. Will shed light on the importance of Vendor qualification and on each and every step involved in the process and the risk assessment. Will cover other related aspects including the Auditing process, Performance monitoring, and the communication process. Learning Objectives are:
- Importance of vendor qualification
- Understanding the vendor qualification program
- Step by step process in the vendor qualification
- Application of Risk assessment
- Audit forms/ checklists and other vendor qualification program documents
- Keys to determine the best potential vendor
- Overview of the auditing process
- Keys to performance monitoring
- Efficient communication processes
Learning Objectives:-
- Importance of vendor qualification
- Understanding the vendor qualification program
- Step by step process in the vendor qualification
- Application of Risk assessment
- Audit forms/ checklists and other vendor qualification program documents
- Keys to determine the best potential vendor
- Overview of the auditing process
- Keys to performance monitoring
- Efficient communication processes
Why Should You Attend?
It is important for the sponsor(s)/ Pharma companies and their compliance personal to understand the process/ steps to the vendor qualification process for FDA regulated companies/ their products. Also, understanding the vendor qualification options, application of risk assessment, the auditing process as well as performance monitoring. This understanding can help identify common pitfalls to avoid when qualifying vendors.
Who Should Attend?
- Internal Auditors
- Compliance officers
- Purchasing Managers
- Quality control Managers
- Quality Assurance Managers
- Senior management
- Regulatory affairs professionals
- Senior management executives (CEO, COO, CFO, etc)
- Regulatory Compliance Associates and Managers
- People investing in FDA-regulated product development projects
