The government is responsible for the control and supervision of traditional (herbal) medicines. This is as stated in Article 1 Number 9, Law Number 36 of 2009 concerning Health. Circulating herbal medicines must go through an assessment, testing, and registration process first. The assessment and testing aim to test efficacy, safety, and quality, meaning they must be tangibly beneficial for healing. Therefore, unregistered herbal medicines are prohibited from being imported, distributed, stored, and consumed because such herbal medicines fall into the dangerous category.
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