1964_PHARMACY_AND_POISONS_ORDINANCE — Page 23

HK Historical Laws 香港歷史法例 All AI Reviewed

CAP. 138]

Pharmacy and Poisons

[1989 Ed.

(c) the ingredients of the medicine and the quantity, dosage and

duration of supply. (Added 58 of 1986 s. 8)

(4) The provisions of subsection (3) shall, in the case of a medicine supplied on a prescription on which the medicine has been supplied by the seller on a previous occasion, be deemed to be complied with if, when the medicine is supplied, the date and the quantity supplied are entered in the book on that day or, if that is not reasonably practicable, on the day next following that day, together with a sufficient reference to an entry in the book duly recording the dispensing of the medicine on the previous occasion.

(5) In the case of a medicine which is supplied or dispensed by a person who is an authorized seller of poisons and is compounded by the person supplying or dispensing it or by a person in his employment, the medicine shall have been compounded by or in the presence of and under the supervision of a registered pharmacist.

[cf. 1933 c. 25 s. 19 U.K.]

28A. Restriction on import and export

of pharmaceutical products

(1) No person shall carry on business as an importer or exporter of pharmaceutical products unless he is registered under this section.

(2) Applications for registration or renewal of registration under this section shall be made in the prescribed manner and shall be accompanied by the prescribed fee.

(3) The Board shall cause a register to be kept in which shall be entered such particulars as the Board may direct in respect of any person whose application for registration under this section is granted or renewed.

(4) An application by any person for registration or renewal of registration under this section may be refused if it appears that, by reason of the inadequacy of the storage facilities used by such person for the storage of pharmaceutical products to be imported or exported by him, it would not be in the public interest to grant the application.

(5) Registration under this section shall be valid for the period beginning on the date of registration and expiring on 30 June next thereafter, and may be renewed within 1 month prior to the expiry of that period.

(6) Any person who contravenes subsection (1) shall be guilty of an offence.

(7) Nothing in this section shall-

(a) apply to any person licensed under this Ordinance as a wholesale

dealer in poisons;

(b) operate so as to prohibit any person who was carrying on business as an importer or exporter of pharmaceutical products

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CAP. 138] Pharmacy and Poisons [1989 Ed. (c) the ingredients of the medicine and the quantity, dosage and duration of supply. (Added 58 of 1986 s. 8) (4) The provisions of subsection (3) shall, in the case of a medicine supplied on a prescription on which the medicine has been supplied by the seller on a previous occasion, be deemed to be complied with if, when the medicine is supplied, the date and the quantity supplied are entered in the book on that day or, if that is not reasonably practicable, on the day next following that day, together with a sufficient reference to an entry in the book duly recording the dispensing of the medicine on the previous occasion. (5) In the case of a medicine which is supplied or dispensed by a person who is an authorized seller of poisons and is compounded by the person supplying or dispensing it or by a person in his employment, the medicine shall have been compounded by or in the presence of and under the supervision of a registered pharmacist. [cf. 1933 c. 25 s. 19 U.K.] 28A. Restriction on import and export of pharmaceutical products (1) No person shall carry on business as an importer or exporter of pharmaceutical products unless he is registered under this section. (2) Applications for registration or renewal of registration under this section shall be made in the prescribed manner and shall be accompanied by the prescribed fee. (3) The Board shall cause a register to be kept in which shall be entered such particulars as the Board may direct in respect of any person whose application for registration under this section is granted or renewed. (4) An application by any person for registration or renewal of registration under this section may be refused if it appears that, by reason of the inadequacy of the storage facilities used by such person for the storage of pharmaceutical products to be imported or exported by him, it would not be in the public interest to grant the application. (5) Registration under this section shall be valid for the period beginning on the date of registration and expiring on 30 June next thereafter, and may be renewed within 1 month prior to the expiry of that period. (6) Any person who contravenes subsection (1) shall be guilty of an offence. (7) Nothing in this section shall- (a) apply to any person licensed under this Ordinance as a wholesale dealer in poisons; (b) operate so as to prohibit any person who was carrying on business as an importer or exporter of pharmaceutical products
Baseline (Original)
222 : CAP. 138] Pharmacy and Poisons [1989 Ed. (c) the ingredients of the medicine and the quantity, dosage and duration of supply. (Added 58 of 1986 s. 8) (4) The provisions of subsection (3) shall, in the case of a medicine supplied on a prescription on which the medicine has been supplied by the seller on a previous occasion, be deemed to be complied with if, when the medicine is supplied, the date and the quantity supplied are entered in the book on that day or, if that is not reasonably practicable, on the day next following that day, together with a sufficient reference to an entry in the book duly recording the dispensing of the medicine on the previous occasion. (5) In the case of a medicine which is supplied or dispensed by a person who is an authorized seller of poisons and is compounded by the person supplying or dispensing it or by a person in his employment, the medicine shall have been compounded by or in the presence of and under the supervision of a registered pharmacist. [cf. 1933 c. 25 s. 19 U.K.] 28A. Restriction on import and export of pharmaceutical products (1) No person shall carry on business as an importer or exporter of pharmaceutical products unless he is registered under this section. (2) Applications for registration or renewal of registration under this section shall be made in the prescribed manner and shall be accompanied by the prescribed fee. (3) The Board shall cause a register to be kept in which shall be entered such particulars as the Board may direct in respect of any person whose application for registration under this section is granted or renewed. (4) An application by any person for registration or renewal of registration under this section may be refused if it appears that, by reason of the inadequacy of the storage facilities used by such person for the storage of pharmaceutical products to be imported or exported by him, it would not be in the public interest to grant the application. (5) Registration under this section shall be valid for the period beginning on the date of registration and expiring on 30 June next thereafter, and may be renewed within 1 month prior to the expiry of that period. (6) Any person who contravenes subsection (1) shall be guilty of an offence. (7) Nothing in this section shall- (a) apply to any person licensed under this Ordinance as a wholesale dealer in poisons; (b) operate so as to prohibit any person who was carrying on business as an importer or exporter of pharmaceutical products
2026-05-05 05:12:02 · Baseline
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222

:

CAP. 138]

Pharmacy and Poisons

[1989 Ed.

(c) the ingredients of the medicine and the quantity, dosage and

duration of supply. (Added 58 of 1986 s. 8)

(4) The provisions of subsection (3) shall, in the case of a medicine supplied on a prescription on which the medicine has been supplied by the seller on a previous occasion, be deemed to be complied with if, when the medicine is supplied, the date and the quantity supplied are entered in the book on that day or, if that is not reasonably practicable, on the day next following that day, together with a sufficient reference to an entry in the book duly recording the dispensing of the medicine on the previous occasion.

(5) In the case of a medicine which is supplied or dispensed by a person who is an authorized seller of poisons and is compounded by the person supplying or dispensing it or by a person in his employment, the medicine shall have been compounded by or in the presence of and under the supervision of a registered pharmacist.

[cf. 1933 c. 25 s. 19 U.K.]

28A. Restriction on import and export

of pharmaceutical products

(1) No person shall carry on business as an importer or exporter of pharmaceutical products unless he is registered under this section.

(2) Applications for registration or renewal of registration under this section shall be made in the prescribed manner and shall be accompanied by the prescribed fee.

(3) The Board shall cause a register to be kept in which shall be entered such particulars as the Board may direct in respect of any person whose application for registration under this section is granted or renewed.

(4) An application by any person for registration or renewal of registration under this section may be refused if it appears that, by reason of the inadequacy of the storage facilities used by such person for the storage of pharmaceutical products to be imported or exported by him, it would not be in the public interest to grant the application.

(5) Registration under this section shall be valid for the period beginning on the date of registration and expiring on 30 June next thereafter, and may be renewed within 1 month prior to the expiry of that period.

(6) Any person who contravenes subsection (1) shall be guilty of an offence.

(7) Nothing in this section shall-

(a) apply to any person licensed under this Ordinance as a wholesale

dealer in poisons;

(b) operate so as to prohibit any person who was carrying on business as an importer or exporter of pharmaceutical products

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