Upon successful completion of this activity, pharmacists should be able to:
- Have a high level understanding of the FDA UDI regulation.
- Determine which products are subject to the FDA UDI rule.
- Understand the modifications that device manufacturers will be making to their product labels and barcodes to comply with the UDI regulation.
- Understand FDA’s position on the future discontinuation of “NDC” and “NHRIC” from device labels.
- Know how to begin moving forward in adopting UDI.