Unique Device Identification (UDI)

This module will provide a broad overview of the Unique Device Identification (UDI) program for the Medtech industry.

English

100% Online

60 Minutes

APACMed Certificate

Assessments

Interactive

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This module has been developed by:

Miang Tanakasemsub 
Head of Regulatory Affairs, APJ Vision
Johnson & Johnson MedTech

About this Module

Purpose
Learning Objectives
Target Audience
Module Structure
Assessment
Certificate

Why should I enrol in this Module?

This module will provide a broad overview of:

  • the UDI system and its anatomy;
  • the fundamental elements of the UDI system;
  • the GUDID data elements; and
  • country specific UDI requirements and implementations

Who should enrol in this Module? 

This Module is suitable for all Regulatory Affairs professionals or anyone with an interest in the regulation of medical devices.

How is this Module structured?

This is a self-paced, interactive Module.  It is divided into a number of individual topics so you can easily track your progress and manage your time.

You must watch all of the videos and presentations before the section will be marked as complete.


You can view the structure and individual topics below.

What kind of assessment do I need to do?

This Module contains a number of short knowledge checks and a final assessment.  

You will have unlimited attempts to pass each knowledge check.

What will I learn?

By the end of this module, you will have an understanding of:

  • the UDI system and its anatomy;
  • the fundamental elements of the UDI system;
  • the GUDID data elements; and
  • country specific UDI requirements and implementations

When will I get my certificate?

At the completion of the course you will immediately have access to the certificate from APACMed.