In this brief exploration into Regulatory Labeling, we will set the stage with the beginnings of regulatory labeling- how and why.
We will then jump forward to the labeling practices of today, highlighting the requirements for labeling in the Medical Device industry. We will encompass the current changes to EU MDR required labeling and the successes and failures we are seeing in industry. Finally, we will end with suggestions to build a robust labeling system and what to get in place to ensure your products don’t end up with a labeling recall.
Learning Objectives:
Identify current US and EU labeling requirements.
Cautions for your labeling program and pitfalls to avoid.