FDA Requirements for Device Labeling: Development, Contents, Distribution, and Changes 2013
23 Aug 2013
Webinar
Description
Topics
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
Who should Attend
Document Control (label generation) professionals
Regulatory Affairs management
Quality Assurance professionals
Design Control professionals
Sales/marketing management
Past Events
FDA Requirements for Device Labeling: Development, Contents, Distribution, and Changes 2013 - 23 Aug 2013, Webinar (39849)
Important
Please, check "FDA Requirements for Device Labeling: Development, Contents, Distribution, and Changes" official website for possible changes, before making any traveling arrangements
