Occupying a critical position in the success or failure of any pharmaceutical product launch, Packaging and Labeling form a bridge between the conception of a product and its realization and distribution. Their activities are also crucial for compliance with regulatory agency requirements.
Still, their importance is often underestimated, especially in the planning phases, which leads to unnecessary increases in cycle time, costly errors, delays in product availability, or product recalls due to noncompliance. Understanding the packaging and labeling process in the larger product development process will provide you an advantage in achieving success.
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