Regulations for Health Risk Assessment Review of Designated Tobacco Products｜第 2 條｜國民健康｜Regulation｜In Force
衛生福利部｜v1.0
Last Amended: 2023-03-22
Manufacturers and/or importers (hereinafter referred to as “the applicants”) shall submit the designated tobacco products (hereinafter referred to as “the products”) to the central competent authority for the health risk assessment review before manufacturing and/or importing the products or within the time limit specified by the central competent authority under Paragraph 2 of Article 7 of this Act. The products with research or test plans that are not in commercialized packaging, not for sale, and in quantities not exceeding the required quantities for research or test are exempted from these regulations with the permission of the central competent authority. The essential components of the products that shall be submitted alongside the products to the central competent authority for the health risk assessment review may be manufactured or imported on a case-by-case basis with the permission of the central competent authority. The application in Paragraph 1 shall be submitted by the importers if the products are manufactured abroad.