BWA- TD - STORAGE AND DISTRIBUTION
ANIMAL PRODUCTION
Botswana / Animal production
FEED SAFETY AND QUALITY
STORAGE AND DISTRIBUTION
questions
2 answers
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text/abstract
Section 28 (extract):
(5) A person authorised in terms of this Act to import, export, distribute, or sell medicines shall not
import, export, distribute, sell, or keep in storage contrary to such conditions as may be prescribed, any
medicine after the date of expiry indicated on the package of the medicine
Section 42 (extract):
(2) Any person who is authorised in terms of this Act to be in possession of Schedule 1A, 1B, 1C, and Schedule 2 medicines, shall store such medicines in a place to which members of the public do not have access and in such manner as may be prescribed.
(3) Any person who is in possession of a prescription preparation shall keep such medicine in a place where children do not normally have access.
Regulation 48:
(1) Medicines shall be stored in secure, well ventilated rooms, with adequate lighting and controlled temperatures.
(2) Schedule 1 medicines shall be kept in bolted steel cabinest or rooms with controlled access.
(3) The storage facilities shall be protected from pests, harsh weather and shall meet building codes,
(4) The guidelines relating to the storage of medicines shall be updated as the Authority determines.
2 answers
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Section 41:
Any medicine imported, manufactured or dispensed within Botswana shall be labelled in accordance with such requirements as the Authority may prescribe.
Regulation 4:
All products manufactured or constituted for the purpose of feeding stock, which are intended for retailing shall, be conspicuously marked)- "This product does not contain any poultry excreta, meat and bonemeal, or any other protein of animal origin"
1 answer
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text/abstract
Section 30 (extract):
(1) No person to whom authorisation has already been granted under this Act shall effect any changes to the manufacturing process, labelling, or packaging of a medicine, except with the prior authorisation of the Authority.
(2) An application for authorisation referred to under subsection (1) shall be in the prescribed form and shall be accompanied by a prescribed fee.