Areas Covered in the Session : - Fundamental areas that must be focused on for supplier management
- Onboarding and sustaining suppliers
- Supplier Qualification based on
- Quality System
- Product Development Process (PDP)
- ISO
- Other regulatory certifications
- Supplier audits
- Criteria for establishing frequency of site audits
- Audit reports and follow up with SCAR (Supplier Corrective Action Requests)
- First article inspection and its correlation to:
- Pre-established SPC (statistical process control)
- CTC (critical to customer)
- CTQ (critical to quality) criteria
- Supplier process control
- Capability assessment for sample inspections
- Role of supplier quality for new product release authorization.
- Supplier’s manufacturing quality plan
- Key areas of focus for supplier quality engineers
- Role of suppliers such as testing laboratories like bio=-compatibility testing labs and suppliers such as sterilization facilities
- Training of suppliers to adhere to your quality expectations
- Regulatory requirements for supplier changes
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| Who Should Attend: - Quality Assurance Departments
- Quality Control Departments
- Research and Development Departments
- Regulatory Affairs Departments
- Manufacturing Departments
- Engineering Departments
- Operations Departments
- Production Departments
- Supplier Auditors
- Supplier Quality Engineers
- Inspection Supervisors
- Supply Chain Departments
- Supplier Managers
- Procurement Managers
- Outside Equipment Manufacturers (OEM)
- Internal Auditors
- Everyone who deals with supply chain management for the medical device industry
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