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Guidelines for the Importation and Exportation of Medicines
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Guidelines for Parallel Importation of Medicines in South Africa
Guidelines for a Licence to Manufacture, Import Export or Distribute Medical Devices and IVDs (MCC: 16.03, July 2016)
Recommendations or licensing requirements for the manufacture, importation, distribution and exportation of Class B, Class C and Class D medical devices. Please note that this is a third-party website. Juta has no control over the nature, content or availability of third-party…
Recommendations for an application for a licence to manufacture, import or export medicines and medical devices. GWP guidelines apply.
Draft regulations to the Medicines Act have been published for a comment period of 3 months. Commentary is due by the 26th April 2017. The draft regulations include the complementary medicines regulations. Medical device-specific regulations (finalised) are published…