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Current Page:Herbal medicinal products

Herbal medicinal products

Research and Development
- Clinical trials
- Good Clinical Practice
Marketing Authorisation or registration (TU) procedures
Pharmacovigilance
Production
- Good Manufacturing Practice
- Qualified person
Distribution
Authorisations
- Authorisation AR 14/12/2006
- Authorisation RD 30/06/2004
Declarations
- Medicines for export
- Manufacturing activity as a sub-contractor
Proper Use

Last updated on 10/02/2023

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