品质

在马来西亚,於1984年药物及化妆品管制条例***下,任何具有医疗作用的药物都必需向马来西亚卫生部申请、注册。

为了符合马来西亚卫生部、执法局的标准,

(a.) Carsis Pharma®佳世士 植物精华油已成功的向 药物管理局(PBKD) 注册,让当局通过注册、品管、审查 的过程,对产品的品质、安全、有效性 进行评估和验证。

(b.) 原料、仓库储存、生产过程、厂地和器材、工作人员的监管都按照、符合药物生产质量管理规范 (GMP) 以确保 产品 符合使用、需求、品质的标准。

*** any product in a dosage unit or otherwise, for use wholly or mainly by being administered to one or more human beings or animals for a medicinal purpose is controlled under Control of Drugs Cosmetic Regulation ( CDCR), Regulation 1984, which promugalated under Sales of Drugs Acts, 1952.

Under the CDCR 1984, Regulation 7(1): Except as otherwise provided in these Regulations, no person shall manufacture, sell, supply, import, possess or administer any product unless:
(a) the product is a registered product; and
(b) the person holds the appropriate licence required and issued under these Regulations.