Packaging and Labeling in Pharmaceutical Product Development – Best Practices

Learning Objectives:

• After completing this course, you’ll be able to:
• Articulate Packaging and Labeling’s role in product development
• Ensure adherence to regulatory agency requirements
• Anticipate potential obstacles in marketing, medical affairs, regulatory, legal or quality assurance
• Work effectively with contract manufacturers or packagers
• Manage labeling in foreign languages
• Avoid unnecessary production costs, back orders and recalls, especially during product launches

Areas Covered in the Session :

• Regulatory requirements for packaging and labeling
• Packaging and labeling interactions
• Putting together the package
• Labeling, “regulated text” and codes
• Errors to avoid
• Special considerations for third-party manufacturers
• Special considerations for product launches
• Potential obstacles and how to overcome them

Who Should Attend:

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