Act No. 13, 2003 MEDICINES AND RELATED SUBSTANCES CONTROL ACT, 2003 a scheduled substance, a controlled chemical, controlled equipment or a medical device (in this definition called goods) to be brought into Namibia, and includes a person who ­ (a) owns the goods brought into Namibia; (b) carries the risk for the goods brought into Namibia; (c) represents to be the one who brought the goods into Namibia or who owns those goods; (d) actually brings the goods into Namibia; (e) is beneficially interested in any way in the goods brought into Namibia; or (f) acts on behalf of a person referred to in paragraphs (a) to (e), and “import” and “importation” have a corresponding meaning; “inspector” means a person authorised as an inspector under section 35; “interchangeable multi-source medicine” means medicine that contains the same quantities of the same active substances in the same dosage form and meets comparable standards as another medicine; “international treaties” means treaties relating to narcotic drugs and psychotropic substances to which Namibia is a party; “label”, when used as a verb, means brand, mark or otherwise designate or describe, and when used as a noun, means a brand or a written, a pictorial or other descriptive matter appearing on or attached to an article or the package containing an article, and referring to the article; “legal practitioner” means a legal practitioner as defined in the Legal Practitioners Act, 1995 (Act No. 15 of 1995); “manufacture” means carry out operations including purchasing of material, processing, packaging, quality control, release and storage of medicinal products and related substances, and “manufacturing” has a corresponding meaning; “manufacturer”, means a person who manufactures or on whose direction manufacturing takes place; “medical device” means any instrument, appliance, material, machine, apparatus, implant or diagnostic reagent used or purported to be suitable for use for medical or veterinary purposes, and includes a part or an accessory of a medical device; “medical practitioner” means a medical practitioner as defined in the Medical and Dental Professions Act, 1993 (Act No. 21 of 1993), or a medical intern as defined in that Act; “medicinal purpose”, in relation to a scheduled substance, means for the purpose of the treatment or prevention of a disease or some other definite curative or therapeutic purpose, but does not include the satisfaction of a habit, or the relief of a craving for the substance used or for any other such substance, except where the substance is administered or used under a programme approved for this purpose by the Minister; “medicine” means ­ (a) a substance or a mixture of substances used or purported to be suitable for use or manufactured or sold for use in ­