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General Regulations

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General Regulations

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CLINICAL TRIAL INVESTIGATORS: (MCC 2.47 V.2, May 2017)

This guideline supplements the guideline on oversight and monitoring of clinical trials to clarify and define the rules of investigators in investigational studies of medical products.

Related Tags (New Search): Medical devices,   Biological medicines,   Medicines

Post-Marketing Reporting of Adverse Drug Reactions to Human Medicinal Products in South Africa (MCC: 2.33, Sept 2016)

The document assist the reporting of adverse drug reactions (ADRs) and in the management of safety data during post-registration and post-marketing clinical trials. To confirm that you have the latest version of this document, please visit: http://www.mccza.com

Related Tags (New Search): Safety,   Adverse Drug Reaction,   Clinical trials,   Medicines

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