Packaging and Labeling in Pharmaceutical Product Development - Best Practices covers topics such as:
- 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
Packaging and Labeling in Pharmaceutical Product Development - Best Practices brings together:
- 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
