FDA Requirements for Device Labeling: Development, Contents, Distribution, and Changes 2013 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 2013 brings together:
- Document Control (label generation) professionals
- Regulatory Affairs management
- Quality Assurance professionals
- Design Control professionals
- Sales/marketing management
