Act No. 13, 2003 MEDICINES AND RELATED SUBSTANCES CONTROL ACT, 2003 (s) as to the transshipment or the importation into, or exportation from, Namibia of a scheduled substance, and specifying the ports or places at which that substance may be imported into, or exported from, Namibia; (t) authorising and regulating the transmission through Namibia of scheduled substances; (u) authorising and regulating the possession by persons or groups of persons entering, or departing from, Namibia of specified quantities of scheduled substances for their own medicinal use; (v) relating to the importation, conveyance, keeping, storage, processing and packing of medicines, and scheduled substances, and the manner in which medicines and scheduled substances must be kept and controlled in different categories of hospitals and health facilities; (w) in consultation with the Minister responsible for the environment, relating to the disposal or destruction of a medicine or a scheduled substance, and the records which must be kept and the reports to be furnished in respect of that medicine or that scheduled substance; (x) relating to the summary seizure and disposal of a scheduled substance found in possession, or under the control, of a person not entitled under this Act to keep or use it; (y) prescribing the methods in accordance with which samples may be taken under this Act and the form of the certificates to be issued by inspectors in respect of those samples; (z) prescribing the methods to be employed, and the form of the certificates to be issued, in connection with the examination or analysis of samples of medicines or scheduled substances, or of any other thing, taken under this Act; (aa) prescribing, in consultation with the Minister responsible for finance ­ (i) the fee payable to the Registrar in respect of the application for registration, and in respect of the registration, of a medicine or a medical device; (ii) the fee payable to the Registrar in respect of the retention of the registration of a medicine or a medical device; (iii) the fee payable for an authorisation granted in terms of section 27(1) for the sale of an unregistered medicine ; (iv) any other fee payable in terms of this Act; and (v) the date on which a fee referred to in this paragraph is payable; (bb) prescribing the registration, and the form and manner of the registration, of medical devices; (cc) regulating or prohibiting the registration, manufacture, modification, importation, storage, transportation, sale, use or destruction of a medical device or category of medical devices;