Supplier qualification and assessment is required in both the QSR regulations and ISO standards. Many companies spend a great deal of time and money in pursuit of compliance with this. Many companies can spend MUCH LESS time and money, and still be in control of their suppliers and in compliance with the regulations. This presentation will review the QSR and ISO requirements for supplier evaluation and assessment, and provide cost efficient, equally compliant options to many of the most common practices.
Areas Covered in the Session:
- QSR and ISO 13485 requirements for supplier selection and assessment
- How to qualify new suppliers in a cost efficient manner
- How to assess current suppliers in a cost efficient manner
- How to perform supplier-related corrective action
- Minimum documentation requirements for supplier qualification, assessment, and related corective action
Who will benefit:
This webinar will provide valuable assistance to all regulated companies that are interested in incurring less cost on supplier evaluation and assessment. The employees who will benefit include:
Jeff Kasoff, RAC, is the Director of Quality at Byrne Medical, a leading manufacturer of endoscopy products. In this position, Jeff is responsible for supplier management, during which he oversees supplier management, CAPA, and document control. Prior to this, Jeff spent 13 years at Life-Tech as the Director of Regulatory Affairs, where he was responsible for regulatory compliance of all aspects of the quality system. Jeff received his regulatory affairs certification in 1996.
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