Skip to site menu Skip to page content

UDI Compliance Guide: Taking the Fear out of FDA Requirements

By Microscan

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.

Enter your details below to view the free white paper

By downloading this whitepaper, you acknowledge that GlobalData may share your information with our white paper partners/sponsors who may contact you directly with information on their products and services.

Visit our Privacy Policy for more information about our services, how GlobalData may use, process and share your personal data, including information on your rights in respect of your personal data and how you can unsubscribe from future marketing communications. Our services are intended for corporate subscribers and you warrant that the email address submitted is your corporate email address.

Related Content