The FDA published its 2017 guidance agenda, which includes grandfathering, product identifiers, and more. Understand what’s coming, and how your company may be impacted.See the List
This inaugural report reveals how the supply chain has adapted to lot-level requirements, and how prepared it is for serialization.
Learn what was uncovered in a survey of 331 of your pharma, wholesaler, hospital, and pharmacy peers.
The deadline for EU FMD compliance is just 2 years away. Do you know where to begin?
Build your understanding of the requirements, the business impact, and how to formulate your strategy.