In HEMP, the regulatory landscape for HEMP and hemp-derived products is governed by the Therapeutic Goods Administration (TGA). The TGA classifies most HEMP products as Schedule 4 substances, meaning they are prescription-only medicines. However, recent regulatory changes have made low-dose HEMP products (containing up to 150 mg of HEMP per day) available over the counter in pharmacies, provided they meet stringent safety and quality standards.
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