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 · Containers, Packages and Identification of Medicinal Products
Medicines Act · 2024 Revised Edition · Part · Containers, Packages and Identification of Medicinal Products
Official textFrom Attorney General's Chambers, unchanged
The Minister may, with the approval of His Majesty the Sultan and Yang Di-Pertuan, make rules imposing such requirements as he considers necessary or expedient with respect to leaflets relating to medicinal products which are supplied, or which are intended to be supplied, with the products, whether by being enclosed in containers or packages of the products or otherwise.
No person shall supply with any medicinal product, or have in his possession for the purpose of so supplying, a leaflet which contravenes any requirements imposed by such rules.
Without prejudice to subsections (1) and (2), no person shall supply with any medicinal product, or have in his possession for the purpose of so supplying, a leaflet which —
medicinal product
“medicinal product” has the meaning ascribed to it by section 4;
falsely describes that product; or
is likely to mislead as to the nature or quality of that product or as to the uses or effects of medicinal products of that description.
medicinal product
“medicinal product” has the meaning ascribed to it by section 4;
Part
Part