UDI rule implementation and compliance guide

Washington, D.C. – The rush to compliance is in full swing. By Sept. 24, 2015, all medical implantable, life-saving or life-supporting devices must comply with the new unique device identifier (UDI) requirements. By 2018 all medicl device makers must be in compliance. It's already clear that implementation and compliance with this new rule is a very big challenge.

You'll need to understand what UDI is … who it applies to … what the exceptions to the rule are … what deadlines you must meet … what UDI issuing agencies are ... and how to work with them.

Implementing UDI is a huge challenge. That's why FDAnews developed the new management report Unique Device Identifier (UDI) Rule Implementation and Compliance Guide. 

It walks you step-by-step through the key portions of the UDI final rule, providing you with all the implementation and compliance details you need to know. 

With Unique Device Identifier (UDI) Rule Implementation and Compliance Guide, you'll gain a clear understanding of this complex new rule and learn to work with it more successfully. You will learn:

• The timetable for implementation
• Which devices must comply with the rule and which do not
• What information must be included on product labels
• How to submit device identification information to the GUDID
• About the accredited UDI issuing agencies and their roles

Unique Device Identifier (UDI) Rule Implementation and Compliance Guide is fully updated to reflect the final rule, chapter by chapter the report includes the critical information you need to get down to the real nitty gritty of complying with the UDI rule. 

Source: FDANEWS