Live Webinar
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FDA Requirements for Device Labeling: Development, Contents, Distribution, and Changes
Date & Time: Tuesday, December 6, 2011
10:00 AM PST | 01:00 PM EST
Duration: 60 Minutes
Instructor: Jeff Kasoff
Location: Online
Price : $245.00
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(for one participant)
Instructor Profile:
Overview:
Jeff Kasoff Director of Regulatory Affairs, Life-Tech, Inc
This webinar is designed for those who perform, supervise, manage, audit, or oversee the creation, approval, control of labels and labeling. Marketing wants to entice customers to buy your product instead of your competitor's! A common method is to make the labeling as eyecatching as possible.
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Prescription Device Labeling Misbranding, False Or Misleading Labeling Approval Issuance Label Integrity Label Inspection Contractor-Produced Labels As A Linkage With Purchasing Controls Retention When a labeling change requires a new submission
Click here to register for this webinar
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 reviews and approves supplier qualification, selection, assessment, and CAPA. 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. ...more
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Who Will Benefit: l
Regulatory Affairs management
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Document Control (label generation) professionals Design Control professionals
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Quality Assurance professionals Sales/marketing management
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