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Supplier Evaluation and Assessment

Supplier Evaluation and Assessment: How to Meet FDA QSR and ISO 13485 Requirements in a Cost-Effective Manner - Webinar By GlobalCompliancePanel

Overview: 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:Regulatory RequirementsKey Elements of a Supplier Qualification ProgramUtilizing Quality AgreementsSupplier AssessmentSupplier NonconformanceRequired DocumentationWho 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:Purchasing ManagementRegulatory ManagementQA ManagementConsultantsJeff Kasoff, RAC, is the Director of Quality at Byrne Medical, a leading manufacturer of endoscopy and colonoscopy devices, where he oversees the operation of the quality system. In this position, Jeff is responsible for oversight of the document control system, including maintenance of regulatory documentation. Prior to this, Jeff spent 13 years at Life-Tech, Inc. as the Director of Regulatory Affairs, where he was responsible for compliance of the corporate quality system. Jeff received his regulatory affairs certification in 1996.GlobalCompliancePanel Phone: 800-447-9407Fax: 302-288-6884


4 Dec 2012 @ 10:00 am

4 Dec 2012 @ 11:00 am

Duration: 1 hours

Timezone: GMT -8:00


Online Webinar

Organised by

GlobalCompliancePanel (deactivated)

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