In force2024 Revised EditionCurrent version · 2024 Revised EditionSee versions on Attorney General's Chambers(opens the publisher’s site)
Medicines Act · 2024 Revised Edition · Part · Miscellaneous and Supplementary Provisions
Medicines Act · 2024 Revised Edition · Part · Miscellaneous and Supplementary Provisions
Official textFrom Attorney General's Chambers, unchanged
The Authority may issue such directions to any person as it thinks necessary for the better carrying out of the provisions of this Act, which may in particular relate to the recall of any registered medicinal product from the market and the disposal of any registered medicinal product.
Authority
“Authority” means the Brunei Darussalam Medicines Control Authority established under section 5;
Any person who contravenes any directions issued by the
Authority under subsection (1) is guilty of an offence.
Authority
“Authority” means the Brunei Darussalam Medicines Control Authority established under section 5;
registered medicinal product
“registered medicinal product” means a product registered in accordance with the provisions of this Act;