Skip to content
In force2024 Revised Edition
Contents

Part · Registration and Licensing

10. Control of manufacture, sale, supply and importation

(1)

Except as otherwise provided in section 18, no person shall manufacture, sell, supply or import any medicinal product unless —

(a)

the medicinal product is a registered product; and

(b)

that person holds the appropriate licence required and issued under this Act.

(2)

The requirement of subsection (1)(b) does not apply to the sale or supply by a retailer of any medicinal product on a general sale list under section 26.

(3)

The provisions of subsection (1) relating to importation do not apply to any person arriving in Brunei Darussalam, who imports, as part of his personal luggage, any medicinal product meant solely for his use or for the use of his family in a quantity not exceeding that which may be reasonably required for one month’s use by one person, or to any public officer importing any medicinal product in the course of his duty, or to any

Medicines 20

person who in accordance with the written consent of the Authority, brings any medicinal product into Brunei Darussalam in transit.

(4)

In subsection (3), “in transit” means taken or sent from any country or territory and brought into Brunei Darussalam by land, air, or water, whether or not landed or trans-shipped in Brunei Darussalam, for the sole purpose of being carried to another country or territory either by the same or another conveyance.

Report

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

Miscellaneous and Supplementary Provisions

Schedules