Understanding and implementing Unique Device Identification (UDI) requirements can be one of the most complex challenges for medical device professionals. In this session, our labeling and regulatory experts will break down the logic behind medical device labeling and guide you through the most common pitfalls that can delay compliance or create costly errors. 

Join us to learn: 

• How to interpret and apply global UDI requirements 

• Common mistakes companies make — and how to avoid them 

• Practical strategies for maintaining compliance across multiple markets 

• Tips for leveraging technology and automation for labeling efficiency 

Whether you’re navigating FDA regulations or submissions, this webinar will help you streamline your labeling process and ensure compliance with confidence.