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This guideline provides information on the reporting and management of adverse events with veterinary medicines. Circular 3.09
This is a draft guideline incorporating medical devices. Not yet finalised
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
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