The Medicines and Related Substances Act 101 of 1965 governs the registration, control, and distribution of medicines, medical devices, and related substances in South Africa. It ensures that all pharmaceutical products meet safety, efficacy, and quality standards before they can be marketed or sold. The Act establishes the South African Health Products Regulatory Authority (SAHPRA) to oversee compliance, safeguard public health, and prevent the sale of substandard or counterfeit products. This legislation plays a critical role in regulating the healthcare sector, protecting consumers, and promoting the responsible use of medicines.
Medicines and Related Sub Act 101 of 1965
R0,00
The Medicines and Related Substances Act 101 of 1965 regulates the registration, sale, and distribution of medicines and medical products in South Africa, ensuring safety, efficacy, and quality standards.
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