Learning Objectives
- Outline the guidelines established by the EU Falsified Medicines Directive.
- Describe how to serialize product and generate reports for EU FMD compliance based on a variety of user roles and scenarios.
- Demonstrate how to view EU Compliance reports.
- Provide a summary of user roles and describe how to add users to TraceLink.
Course Length
Who should take this course
Virtual manufacturers selling product into EU markets
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