FDA Requirements for Device Labeling: Development, Contents, Distribution, and Changes

Why You Should Attend:

Your  company's marketing department 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. Sometimes mislabeling and aggressive labeling can put you in to trouble.

This FDA labeling webinar will provide a comprehensive knowledge of labeling development and subsequent control. The updated FDA requirements and expectations regarding labeling contents will be covered. We will discuss the recommended best practices  and how to follow it to assure substantial compliance. 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 compliance.

Areas Covered in the seminar:

• 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