【法规名称】
【法规编号】 44128 什么是编号？
【正 文】
第2页 CAP 134A DANGEROUS DRUGS REGULATIONS
|
[接上页] (b) he shall use a separate register or separate part of the register for entries made with respect to each of the dangerous drugs specified in paragraph 1 of Part I of the First Schedule to the Ordinance or in paragraph 2, 3, 4, 5, 6 or 7 thereof and for this purpose- (i) each such drug shall be deemed to comprise its salts and any preparation, admixture, extract or other substance containing any proportion of it or its salts; and (ii) any isomer of a dangerous drug the existence of which is possible within its specific chemical designation shall be deemed to be identical with that drug;(c) he shall use a separate page within the register or separate part of the register for entries made with respect to different dangerous drugs and different strengths of preparations comprised within the class of dangerous drugs to which that register or separate part relates. (L.N. 191 of 1996)(2) (Repealed L.N. 191 of 1996) (3) Where a registered medical practitioner, a registered dentist, a registered veterinary surgeon or a specified person obtains or supplies any dangerous drug (which, in the case of the specified person, means a specified dangerous drug) packed in ampoules, he shall be deemed to have complied with the requirements- (2 of 1992 s. 13; L.N. 556 of 1997) (a) of paragraph (1) in regard to entry in the register required to be kept under that paragraph of true particulars with respect to every quantity of every dangerous drug obtained or supplied; or (b) (Repealed L.N. 191 of 1996)if he enters as the amount which he has obtained or supplied, as the case may be, true particulars as to either the total quantity of the dangerous drug or the total quantity thereof intended to be administered or injected. (4)-(5) (Repealed L.N. 191 of 1996) (6) (a) Subject to sub-paragraph (c), a manufacturer of any preparation specified in Part II of the First Schedule to the Ordinance and a wholesale dealer in any such preparation shall keep every invoice or other like record issued in respect of each quantity of any such preparation obtained by him and in respect of each quantity of any such preparation supplied by him. (b) A retail dealer in any such preparation shall keep every invoice or other like record issued in respect of each quantity of any such preparation obtained by him. (c) Sub-paragraph (a) does not apply in the case of a preparation manufactured by a registered medical practitioner, or by a person referred to in subsection (5) of section 22 of the Ordinance, under the authority conferred by sub-section (4) or (5) of the said section 22, as the case may be.(7) Any person who contravenes any of the provisions of paragraph (1) or (6) shall be guilty of an offence and shall be liable on conviction to a fine of $450000 and to imprisonment for 3 years. (L.N. 191 of 1996; L.N. 201 of 1996) (8) It is a defence for a person charged with committing an offence under paragraph (7) in relation to paragraph (1) to show that he took all reasonable steps and exercised all due diligence to avoid committing the offence. (L.N. 288 of 1996) [cf. S.I. 1964/1811 reg. 17 U.K.] Cap 134A reg 6 Requirements as to registers The following requirements shall be complied with by any person required to keep a register under regulation 5, that is to say- (a) there shall be specified at the head of any page of such register- (i) the class of dangerous drugs; and (ii) where applicable, the particular dangerous drug and the particular strength of the preparation comprised within such class, to which the entries on that page relate; (L.N. 191 of 1996)(b) every entry required to be made under regulation 5 in such register shall be made on the day on which the dangerous drug is received or, as the case may be, on which the transaction with respect to the supply of the dangerous drug by the person required to make the entry takes place, or, if that is not reasonably practicable, on the day next following the said day; (c) no cancellation, obliteration or alteration of any such entry shall be made, and every correction of such an entry shall be made only by way of a marginal note or footnote which shall specify the date on which the correction is made; (d) every entry required to be made under regulation 5 in such register, and every correction of such an entry, shall be made in ink or otherwise so as to be indelible; (e) such a register shall not be used for any purpose other than the purposes of the Ordinance; (f) such person shall if so required by the Director or any public officer authorized in writing by the Director in that behalf- (i) furnish such particulars as may be required with respect to the obtaining or supplying by him of any dangerous drug, or with respect to any stock of dangerous drugs in his possession; (ii) for the purpose of confirming any such particulars, produce any stock of dangerous drugs in his possession; and (iii) produce such register and such other books or documents in his possession relating to any dealings in dangerous drugs as may be required;(g) a separate register shall be kept in respect of each set of premises at which the person required to keep the register carries on business, but save as aforesaid not more than one register shall be kept at one time in respect of each class of dangerous drug in respect of which he is required to keep a separate register or part of a register, so, however, that a separate register may, with the approval of the Director, be kept in respect of each department of the business carried on by him; |
- 此法规有错误，我来纠正。请点击在此 提交错误内容或者您纠正的内容！