Speeches
LC: Speech by SFH on Pharmacy and Poisons Ordinance
Following is the speech (English translation) by the Secretary for Food and
Health, Dr York Chow, in moving the motion on Pharmacy and Poisons
(Amendment)(No.3) Regulation 2008 and Poisons List (Amendment)(No.3)
Regulation 2008 under the Pharmacy and Poisons Ordinance (Cap. 138) in the
Legislative Council today (July 3):
Madam President,
I move that the motion under my name, as printed on the Agenda, be passed.
Currently, we regulate the sale and supply of pharmaceutical products
through a registration and monitoring system set up in accordance with the
Pharmacy and Poisons Ordinance. The Ordinance maintains a Poisons List under
the Poisons List Regulations and several Schedules under the Pharmacy and
Poisons Regulations. Pharmaceutical products put on different parts of the
Poisons List and different Schedules are subject to different levels of
control in regard to the conditions of sale and keeping of records.
For the protection of public health, some pharmaceutical products can only
be sold in pharmacies under the supervision of registered pharmacists and in
their presence. For certain pharmaceutical products, proper records of the
particulars of the sale must be kept, including the date of sale, the name
and address of the purchaser, the name and quantity of the medicine and the
purpose for which it is required. The sale of some pharmaceutical products
must be authorised by prescription from a registered medical practitioner,
dentist or veterinary surgeon.
Arising from an application for registration of two pharmaceutical products,
the Pharmacy and Poisons Board proposes to add maraviroc and its salts, as
well as nilotinib and its salts, to Part I of the Poisons List and the First
and Third Schedules to the Pharmacy and Poisons Regulations. Pharmaceutical
products containing these two substances must then be sold in pharmacies
under the supervision of registered pharmacists and in their presence, with
the support of prescriptions.
We propose that these amendment regulations take immediate effect upon
gazettal on July 4, 2008 to allow early control and sale of the relevant
medicine.
The two Amendment Regulations are made by the Pharmacy and Poisons Board,
which is a statutory authority established under the Ordinance to regulate
pharmaceutical products. The Board comprises members engaged in the
pharmacy, medical and academic professions. The Board considers the proposed
amendments necessary in view of the potency, toxicity and potential side
effects of the medicines concerned.
With these remarks, Madam President, I move the motion.
Ends/Thursday, July 3, 2008
Issued at HKT 17:10
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