- Overview
- A National or European Scheme
- Scope of the Directive
- Traditional use
- Safety
- The positive list and Committe for Herbal Medicinal products
- Registration
- Manufacturing
- Qualified Persons (QPs)
- Responsible Persons (RPs)
- Quality requirements
- Distribution
- Importation
- Inspections
- Information
- Review of the Directive
- Timetable and transitional arrangements
- Changes to the existing regulatory arrangements
- Fees
- Regulatory impact
