Supevision of Wholesale distribution
According to the Pharmaceutical Law, activities of purchasing, selling or storing medicinal products are regulated. Therefore the Chief Pharmaceutical Inspector issues authorisations to run pharmaceutical wholesale stores, consignment warehouses and customs warehouses for storage of medicinal products.
In order to obtain such authorisation, a relevant application must be submitted to the Chief Pharmaceutical Inspector. The authorisation may be granted to entrepreneurs who meet the requirements specified in Chapter 6 of the Pharmaceutical Law Act.
Wholesale of medicinal products may be conducted only as specified in the Pharmaceutical Law Act and it is supervised by the Chief Pharmaceutical Inspector.
EudraGMDP is an EU database referred to in 111 ( 6 ) of Directive 2001/83/EC and Article 80 ( 6 ) of Directive 2001/82/EC. The database contains information on granted manufacturing authorisations and certificates for entrepreneurs that manufacture, import or distribute medicinal products, active pharmaceutical ingredients and excipients used in manufacturing of medicinal products.