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This is a draft guideline incorporating medical devices. Not yet finalised
This guideline provides information on the reporting and management of adverse events with veterinary medicines. Circular 3.09
This document provides information on the record of medicines and covers notification for initiations of a recall, information required for assessment of a recall, classification, communications and procedures.
Related Tags (New Search): Recalls
RECALL, ADVERSE EVENT and POST-MARKETING VIGILANCE REPORTING of MEDICAL DEVICES and IVDs (MCC 8.04, Aug 17)
Guidelines on the recall, adverse event reporting and post-marketing vigilance of medical devices and IVDS in South Africa