Meeting compliance requirements for the FDA Unique Device Identification (UDI) rule is priority-one for today’s medical device manufacturers and labellers.
With compliance dates on the horizon for new classes of devices, businesses must be proactive in ensuring standardized product serialization and update their labelling procedures at a rapid pace, or forfeit the right to participate legally in the marketplace.
The pressure to meet this demand can be daunting, and understanding the available UDI documentation can also be a formidable challenge to the new UDI adopter.
This whitepaper offers guidelines for simplifying each step toward UDI compliance and answers common questions about the UDI rule.
Download to find out more.