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 · Registration and Licensing
Medicines Act · 2024 Revised Edition · Part · Registration and Licensing
Official textFrom Attorney General's Chambers, unchanged
The Authority may, without assigning any reason, reject any application for the registration of any medicinal product.
Authority
“Authority” means the Brunei Darussalam Medicines Control Authority established under section 5;
Authority
“Authority” means the Brunei Darussalam Medicines Control Authority established under section 5;
medicinal product
“medicinal product” has the meaning ascribed to it by section 4;
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