Pharmaceutical companies are legally and ethically obligated to make available the most up to date information on how to use their products safely on the label for healthcare professionals and patients. Because the regulatory requirements, labeling is a very critical component of a product registration dossier. Once approved, it serves as the document that tells a complete story about the product. Labeling provides compressive information on a product and determines the proper treatment for the patient. Packaging plays a huge role in keeping the drug and device from contamination safe for its patients and users.

Labeling is not only one of the most complex, cross-functional processes within the pharmaceutical industry. It is one of the most common areas of inspection findings and it is critical to have an end-to-end labeling to packaging process to ensure patient safety. This year, the 2nd Safety Labeling and Packaging Summit will explore best practices to develop and enhance an end-to-end process to ensure a compliant label for your drug packaging.