Transferring a Medical OEM Molding and Assembly Operation to a Manufacturer With Validated Systems and Processes 2013 is a webinar that covers topics such as:
- Developing a Master Validation Plan
- Procedures to transfer equipment and processes to another facility in-house or to a supplier
- Gathering of data for a gap analysis
- Developing Quality Plan
- Validations and quality procedures
- Risk management
- The transfer plan: The tool transfer, The equipment transfer and The assembly transfer
- Choose the right "World Class" quality supplier
- Multi-functional team approach/responsibility
- Validations and quality procedures
- Pit falls and downsides
- Operations, quality and validations
- Conduct a "Lessons Learned Program"
Transferring a Medical OEM Molding and Assembly Operation to a Manufacturer With Validated Systems and Processes 2013 brings together:
- Manufacturing engineers
- OEM plant managers and operation personnel in the medical industry
- QA, Regulatory Affairs and validation teams
- R&D, product development engineers and managers associated with validation of new products
- Senior management
- Validation specialists
- Suppliers to the medical industry
- Suppliers entering into the medical industry
- Corporate auditors
- Consultants
