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[接上页] (3) In a case where a substance included in the First Schedule is supplied, a record shall be kept on the premises in such a way that there can readily be traced at any time during a period of 2 years after the date on which the substance was supplied the following particulars- (a) the name and quantity of the poison supplied; (b) the date on which the poison was supplied; (c) the name and address of the person to whom the poison was supplied; and (d) the name of the person who supplied the poison or who gave the prescription upon which it was supplied.(4) The container of the medicine shall be labelled- (a) with a designation sufficient to identify the institution or veterinary institution from which it was supplied; (L.N. 137 of 1978) (b) except in the case of a medicine made up ready for treatment, with the word "Poison 毒药"; (c) in the case of a poison supplied from a veterinary institution, with the words "For animal treatment only 只限医治禽畜用".(5) The medicine shall be clearly labelled with instructions for use in English and in Chinese. (6) In the case of a medicine to which regulation 16 applies the requirements of that regulation shall be satisfied in addition to the requirements of this regulation. Cap 138A reg 23 Supply of medicines for use in institutions, etc. (1) In any institution in which medicines are dispensed in a dispensing or pharmaceutical department in charge of a registered pharmacist or any other person approved by the Director of Health for that purpose, no medicine containing a poison shall be supplied from that department, except in cases of emergency, for use in the wards, operating theatres or other sections of the institution, except in accordance with paragraphs (2) and (3). (L.N. 76 of 1989) (2) Subject to paragraph (4), the medicines shall not be supplied except upon a written order signed by a duly registered medical practitioner, registered dentist, or by a person authorized to be in charge of a ward, theatre or other section of the institution. (3) The container of the medicine shall be labelled- (a) with words describing its contents; (b) in the case of substances included in the First Schedule, with a distinguishing mark or other indication indicating that the poison is to be stored in a cupboard reserved solely for the storage of poisons.(4) In the case of an emergency, a medicine containing a poison may be supplied without a written order if the person ordering the medicine undertakes to furnish a written order in respect of that medicine within the next 24 hours. Cap 138A reg 24 Storage of poisons in institutions (1) In any institution in which medicines are dispensed in a dispensing or pharmaceutical department in the charge of a person appointed for the purpose, all poisons other than those issued for use within the institution shall be stored in that department. (2) In any institution to which paragraph (1) does not apply all poisons other than those issued for use within the institution shall be stored- (a) in the charge of a person appointed for the purpose by the governing body or person in control of the institution; and (b) in the case of substances included in the First Schedule either in a cupboard or drawer, or on a shelf, reserved solely for the storage of poisons.(3) No poison shall be stored on an open shelf, unless the container of the poison is distinguishable by touch from the containers of any other substances stored in the same premises. (L.N. 137 of 1978) (4) In every institution, every substance in the First Schedule which is stored in the wards shall be stored in a locked cupboard reserved for the storage of poisons. (L.N. 137 of 1978) (5) All places in which poisons are required by this regulation to be stored shall be inspected at regular intervals of time not exceeding three months by a registered pharmacist or registered medical practitioner appointed for the purpose by the governing body of the institution and a record of all inspections shall be made in a book kept at the institution. Cap 138A reg 24A Applications to be entered on list under section 25 PART VA LISTED SELLERS OF POISONS (1) Any application under section 25(1) shall be made in writing to the Committee and shall be accompanied by the fee specified in the Ninth Schedule. (2) The Committee may grant or refuse any application under this regulation and shall notify the applicant of its decision: Provided that if the Committee intends to refuse an application the Committee shall first notify the applicant and the applicant may, not later than 14 days after the date of such notification, submit representations in writing to the Committee in support of his application. (3) Where the Committee grants an application under this regulation the Committee shall notify the Board of its decision and shall state whether the applicant has paid the prescribed fee. (4) Any person aggrieved by a decision of the Committee under this regulation may, in the prescribed manner, appeal to the Tribunal against that decision. |