The efforts of professionals in medical product labeling and related disciplines are key to providing essential information needed by providers, patients, and payers, to make decisions about product access, prescription, and use. Influences such as digital technology, patient-centricity, evolving product classes, and changing regulations require the use of informed, systematic approaches throughout the labeling cycle to ensure the development and availability of current, compliant information in all regions where products are marketed.

At the conference, you'll learn from regulators and industry peers, update your knowledge of key local and global labeling policies, and examine the impact of changes on regulatory compliance. Most importantly, through interactive discussions with expert panels and peer-to-peer exchange, you’ll share approaches, processes, and tools to broaden understanding and ensure the availability of effective labeling content that meets the needs of patients, consumers, and prescribers.