Makes provision for the determining of new schedules and the making ofĮstablishes the South African Medicines and Medical Devices Regulatory Authority Provisions retain regulations made and schedules determinedĪct and the Stock Remedies Act, but schedules 1 to 9 of the 1965 Act are Schedules 1 to 9 identify regulated substances. Regulations is an essential component of the regulatory system established Of medicines for human and animal use and the making of other Manufacture, the sale and possession of substances in the various schedules.
Manufacture, sale and possession of medicines for human and animal use be Made material amendments to the Stock Remedies Remedies Act, 36 of 1947 (the Stock Remedies Act). Governed by the Fertilizers, Farm Feeds, Agricultural
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The registration and control of agricultural substances and stock remedies were The Medicines and Related Substances Control Act, 101 of 1965 (the 1965 Act). Of medicine for human and animal use were governed by The application was brought were as follows. Issued by the Minister of Health and purported to provide schedules to the Act Regulatory Authority Act, 132 of 1998 (the Manufacturers Association of South Africa and the Crop Protection and Animalīy the President and purported to bring into operation the South African South Africa, the Minister of Health, the Minister of Agriculture, certainįunctionaries in the Departments of Health and Agriculture, It began asĪn application to the Transvaal High Court by the President of the Republic of Question whether a court has the power to review and set aside a decision by theīring an Act of Parliament into force. PHARMACEUTICAL MANUFACTURERS Seventh Applicant THE REGISTRAR OF MEDICINES Third ApplicantĬHAIRPERSON, MEDICINES CONTROL COUNCILğourth Applicant Pharmaceutical Manufacturers Association of South Africa and Another: In re Ex Parte President of the Republic of South Africa and Others (CCT31/99) Z(2) SA 674 2000 (3) BCLR 241 (25 February 2000)
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