Medicines Act · 2024 Revised Edition · Part · Brunei Darussalam Medicines Control Authority
6. Functions of Authority
Official textFrom Attorney General's Chambers, unchanged
The functions of the Authority are to advise the Minister upon and to make decisions and recommendations in relation to —
Authority
“Authority” means the Brunei Darussalam Medicines Control Authority established under section 5;
any matter related to any registration, the issue of any licence or the listing of any medicinal product;
the amendment of the Schedule;
the making, amendment or any revocation of any rules under this Act;
Medicines 18
any matter with regard to the import, export, manufacture, storage, handling, distribution, sale, supply, possession, use, labelling or disposal of medicinal products, or that the Authority thinks fit or that the Minister may refer to it;
the establishment of sub-committees to consider specific issues, including those relating to traditional or herbal medicines, cosmetics and the like.
Terms defined in s 2
Authority
Defined · s 2“Authority” means the Brunei Darussalam Medicines Control Authority established under section 5;
labelling
Defined · s 2“labelling”, in relation to a container or package of medicinal products, means affixing to or otherwise displaying on it a notice describing or otherwise relating to the contents;
medicinal product
Defined · s 2“medicinal product” has the meaning ascribed to it by section 4;
Part
Registration and Licensing
Part
Clinical Trials
Part
Sales and Other Dealings of Medicinal Products
Part
Pharmacies
Part
Containers, Packages and Identification of Medicinal Products
Part
Promotion of Sales of Medicinal Products and Medical Advertisements
Part