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medicines and related substances control act 101 of 1965

medicines and related substances control act 101 of 1965

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21. Definitions(1) In this Act, unless the context otherwise indicates-'advertisement', in relation to any medicine or Scheduled substance, means any written, pictorial, visualor other descriptive matter or verbal statement or reference-(a) appearing in any newspaper, magazine, pamphlet or other publication; or(b) distributed to members <strong>of</strong> the public; or(c) brought to the notice <strong>of</strong> members <strong>of</strong> the public in any manner whatsoever,which is intended to promote the sale <strong>of</strong> that medicine or Scheduled substance; <strong>and</strong> 'advertise' has acorresponding meaning;'analyst' means an analyst to whom authority has been granted under section 27;'approved name', in relation to a medicine, means the international non proprietary name (INN) <strong>of</strong> suchmedicine or, where no such name exists, such other name as the council may determine, not being a br<strong>and</strong>name or trade name registered in terms <strong>of</strong> the Trade Marks Act, 1993 (Act 194 <strong>of</strong> 1993);'certificate <strong>of</strong> registration' means a certificate <strong>of</strong> registration issued under section 15 (4), 15A (4) or 15(B) (4);'council' means the Medicines Control Council established by section 2;'dentist' means a person registered as such under the Health Pr<strong>of</strong>essions Act, 1974;'Director-General' means the Director-General: Health;'export' includes deliver or supply within the Republic for dispatch to any destination outside theRepublic;'hospital' means any institution established as a hospital or a nursing home or registered as such in terms<strong>of</strong> any law;'immediate container', in relation to a medicine or Scheduled substance, means a container which is indirect cont<strong>act</strong> with the medicine or substance;'interchangeable multi-source medicine' means <strong>medicines</strong> that contain the same <strong>act</strong>ive <strong>substances</strong>which are identical in strength or concentration, dosage form <strong>and</strong> route <strong>of</strong> administration <strong>and</strong> meet thesame or comparable st<strong>and</strong>ards, which comply with the requirements for therapeutic equivalence asprescribed;'inspector' means a person authorized as such under section 26;'label', when used as a verb, means br<strong>and</strong>, mark or otherwise designate or describe, <strong>and</strong> when used as anoun, means any br<strong>and</strong> or mark or any written, pictorial or other descriptive matter appearing on orattached to or packed with <strong>and</strong> referring to any article or the package containing any article;'magistrate' means a magistrate as defined in section 1 <strong>of</strong> the Magistrates Act. 1993 ( Act No.90 <strong>of</strong>1993), <strong>and</strong> includes an additional magistrate <strong>and</strong> an assistant magistrate;

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