Regulation 2

In this Order, unless the context otherwise requires —“health product” has the same meaning as in the Health Products Act (Cap. 122D);“health product manufacturer’s licence” means a manufacturer’s licence mentioned in section 12 of the Health Products Act;“import licence” means an import licence mentioned in section 5(2) of the Act;“importer’s licence” means an importer’s licence mentioned in section 13 of the Health Products Act;“licensed retail pharmacy” means premises specified in a pharmacy licence;“medicinal product” means a medicinal product that falls within the category of a therapeutic product on or after 1 November 2016;“medicine manufacturer’s licence” means a manufacturer’s licence mentioned in section 6(2) of the Act;“Medicines Exemption Order” means the Medicines (Traditional Medicines, Homoeopathic Medicines and other Substances) (Exemption) Order (O 6);“pharmacy licence” means a licence issued under the Health Products (Licensing of Retail Pharmacies) Regulations 2016 (G.N. No. S 330/2016);“product licence” means a product licence mentioned in section 5(1) of the Act;“Register of Health Products” has the same meaning as in the Health Products Act;“registrant”, in relation to a registered therapeutic product, means a person who has applied for and obtained the registration of the therapeutic product under the Health Products Act;“therapeutic product” means a health product categorised as a therapeutic product in the First Schedule to the Health Products Act;“Therapeutic Products Regulations” means the Health Products (Therapeutic Products) Regulations 2016 (G.N. No. S 329/2016);“wholesale dealer’s licence” means a wholesale dealer’s licence mentioned in section 6(3) of the Act;“wholesaler’s licence” means a wholesaler’s licence mentioned in section 14 of the Health Products Act.