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Conference

FDA Requirements for Device Labeling: Development, Contents, Distribution, and Changes - Webinar By GlobalCompliancePanel

About this event

Web site
bit.ly/szkxtF…
When
6 Dec 2011
Where
Online Training, online training, United States
Organiser
GlobalCompliancePanel
Contact address
webinars web
online training webinar
Suite 1200
Wilmington
Delaware
United States
Tel
18004479407
Fax
3022886884
E-mail
webinars@globalcompliance…

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 eye-catching as possible. Be careful! You need to know what information can (and more importantly) CANNOT be present on the labeling. This presentation provides comprehensive knowledge of labeling development and subsequent control. FDA requirements and expectations regarding labeling contents will be covered, as will recommended practices to assure substantial compliance.

Areas Covered in the Session:
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
Who Will Benefit:
Regulatory Affairs management
Document Control (label generation) professionals
Design Control professionals
Quality Assurance professionals
Sales/marketing management

Price List:
Live : $245.00
Corporate live : $995.00
Recorded : $295.00

webinars@globalcompliancepanel.com
http://www.globalcompliancepanel.com

Phone: 800-447-9407
Fax: 302-288-6884