s 10 Register of medicinal products and import licence
10.—(1) The licensing authority must maintain a register in which must be entered all medicinal products in respect of which product licences have been granted and remain in force. (2) The register must be in such form and contain such particulars as the licensing authority may determine. (3) The licensing authority may, on application by a person who is not the holder of a product licence, grant an import licence to that person to import any medicinal product for sale or supply where the licensing authority is satisfied that that product is in all respects the same as a medicinal product registered under subsection (1).