Complying with international requirements and standards to ensure global UDI compliance is a key challenge for medical device manufacturers. Contending with changing deadlines and often ambiguous guidelines, manufacturers are looking for clarity from regulators on what exactly is required of them.
In light of this and the delay to EUDAMED, Pharma IQ have created a post-show report highlighting the most exciting takeaways from the 2019 Global UDI and Master Data Forum.
Download the full report now >>
Other key benefits of downloading the report:
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