Packaging and Labeling in Pharmaceutical Product Development - Best Practices

Key Topics

• Articulate Packaging and Labeling’s role in product development
• After completing this course, you’ll be able to:
• Anticipate potential obstacles in marketing, medical affairs, regulatory, legal or quality assurance
• Ensure adherence to regulatory agency requirements
• Manage labeling in foreign languages
• Work effectively with contract manufacturers or packagers
• Regulatory requirements for packaging and labeling
• Avoid unnecessary production costs, back orders and recalls, especially during product launches
• Putting together the package
• Packaging and labeling interactions
• Errors to avoid
• Labeling, "regulated text" and codes
• Special considerations for product launches
• Special considerations for third-party manufacturers
• Potential obstacles and how to overcome them

Who should Attend

• Regulatory Affairs Departments
• Operations Departments
• Quality Assurance Departments
• Labeling and Packaging Departments
• Packaging Technology Departments
• Production Control Departments
• Package Engineering Departments
• Labeling Coordination Departments
• Project Management
• Packaging Operations Departments
• Sales and Marketing Departments