in Tag: Importers  (clear all)


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Guidelines for the Importation and Exportation of Medicines (MCC: 5.01, Jun 2011)

Guidelines for the Importation and Exportation of Medicines

Related Tags (New Search): Exporters,   Importers

POSITION STATEMENT: TRANSITIONAL ARRANGEMENTS FOR MEDICAL DEVICES (MCC 9.96, JUN 2017)

Please note that this is a third-party website. Juta has no control over the nature, content or availability of third-party websites, and shall not be liable, in any manner whatsoever, for any damages incurred through the use of third-party websites.

Related Tags (New Search): Licencing,   Medical devices,   IVDs,   Importers,   Wholesaler,   Manufacturers

Guidelines for Parallel Importation of Medicines in South Africa (MCC: 5.02, Jun 2003)

Guidelines for Parallel Importation of Medicines in South Africa

Related Tags (New Search): Exporters,   Importers

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…

Related Tags (New Search): GMP,   IVDs,   Licencing,   Medical devices,   Classification,   Conformity assessment,   Safety and performance,   Fees,   Classification,   Importers,   Distributor

Guidelines for Licence to Manufacture, Import or Export (MCC: 16.01, Feb 2004)

Recommendations for an application for a licence to manufacture, import or export medicines and medical devices. GWP guidelines apply.

Related Tags (New Search): Inspections,   GWP,   Inspections,   Complementary medicines,   MCC Inspections,   Licensing,   Application,   Fees,   Exporters,   Importers,   Manufacturers,   Medicines

Medicines and Related Substances Act 101 of 1965, Draft Regulations GG 40577, 27 January 2017

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…

Related Tags (New Search): Allopathic medicines,   Complementary medicines,   Health supplements,   Exporters,   Importers,   Distributor,   Manufacturers,   Community pharmacy,   Institutional pharmacy,   Regulations