Meeting Designed For

• Labeling
• Regulatory Affairs/Drug Review and Approval Process
• Clinical Safety/Pharmacovigilance
• Pharmacoepidemiology
• Medical Affairs and Communications
• Medical Writing
• Clinical Research and Development
• Product Research and Development Alliances
• Quality Control/Quality Assurance
• Marketing/Advertising/Promotion
• Supply Chain
• Patient Advocacy
• Packaging

At the completion of this conference, the participant should be able to:

• Discuss global labeling regulations and trends, including updates from key regions and emerging initiatives, such as e-labeling and healthcare interoperability
• Explain ways to ensure labeling compliance with regulatory requirements by applying best practices that uphold labeling accuracy, safety, and consistency across global markets
• Recognize the role of advanced technologies, such as AI, ML, and NLP in streamlining labeling processes and improving efficiency
• Discuss how to incorporate patient perspectives and health literacy principles into labeling practices to improve accessibility and understanding among diverse patient populations
• State techniques to optimize end-to-end labeling through effective governance, traceability, and lifecycle alignment from development to compliance
• Recognize ways to address specialized labeling challenges, such as CGT and rare diseases, by leveraging new guidelines and stakeholder collaboration
• Describe areas to build upon key professional development skills, including leadership, compliance, and adaptability