The staff of the information centre will be happy to answer your general questions.
Details of distribution of pharmaceuticals
- Notification of the commencement of distribution activities within the territory of the Czech Republic based upon distribution authorization for medicinal products issued by another EU member state - after Brexit
- Conditions governing the conduct of distribution activities within the territory of the Czech Republic
- Reporting of medicinal products
Questions and answers
- 11. What can be a terminal (cross-dock) in connection with the distribution activity?
- 10. What should be done when the batch number of a supplied medicinal product does not correspond with the delivery documentation (delivery notes, invoices ...)?
- 9. Must all supplies of medicinal products accompanied by a certificate of analysis (CoA) and / or batch release certificate by the manufacturer of the medicinal product (CoC)?
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