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- Approval and follow-up of marketing authorisation (MA)
- Classification of medicinal products
- Clinical trials of medicines for human use
- Import and wholesaling of medicines
- Pharmacovigilance information for the marketing authorisation holders
- Pricing of medicines
- Single technology assessments of medicines
- Guidance and regulations
- Development and manufacturing of medical devices
- Supply, import and distribution
- Clinical investigation of medical devices
- Performance studies of in vitro-diagnostic medical devices (IVDs)
- Reporting of serious incidents involving medical devices
- Norwegian register for devices and EUDAMED
