EU Labeling of Human Tissue and Cells: How Will You Sustain Compliance?

As of April 29, 2017, organizations within the European Union (EU)—as well as companies that do business in the EU—must have a single European code (SEC) on all donated tissues and cells used for human application. Failure to comply can result in fines, confiscation of materials and health risks to patients. What can you do to ensure compliance with this important regulation?

Get the answers you need from experts Jay Crowley from USDM Life Sciences and Guenther Martin from Loftware as they address your key questions in this informative Q&A Report including:

• What are the new coding requirements and what is the correct format? 
  
• Are there any tissue and cells exempted from the requirement? 
  
• How will the regulation impact other medical device labeling? 
  
• How can you leverage existing UDI labeling to comply with the SEC? 
  

Learn how you can meet this new requirement while optimizing your labeling process. Download it now!