FDA Requirements for Device Labeling: Development, Contents, Distribution, and Changes - Webinar by GlobalCompliancePanel 2011

  • 04 Aug 2011
  • Webinar

Description

FDA Requirements for Device Labeling: Development, Contents, Distribution, and Changes is a webinar that covers topics such as:

  • Misbranding, False Or Misleading Labeling
  • Prescription Device Labeling
  • Issuance
  • Approval
  • Label Inspection
  • Label Integrity
  • Retention
  • Contractor-Produced Labels As A Linkage With Purchasing Controls
  • When a labeling change requires a new submission


FDA Requirements for Device Labeling: Development, Contents, Distribution, and Changes brings together Document Control (label generation) professionals, Regulatory Affairs management, Quality Assurance professionals, Design Control professionals and Sales/marketing management.

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Important

Please, check "FDA Requirements for Device Labeling: Development, Contents, Distribution, and Changes - Webinar by GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Legal, Marketing & Sales, Quality assurance
Health & Medicine: Pharma
Industry: Food & Beverages

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