in Tag: Recalls  (clear all)


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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

Related Tags (New Search): Medical devices,   IVDs,   Recalls

Veterinary Drug Recalls (MCC: 3.10, Jan 2004)

This guideline provides information on the recall of veterinary medicines. Circular 3.10

Related Tags (New Search): Recalls,   Adverse Drug Reaction,   Adverse Drug Event,   Veterinary medicine

Guideline on Veterinary Drug Adverse Events (MCC: 3.09, Jan 2004)

This guideline provides information on the reporting and management of adverse events with veterinary medicines. Circular 3.09

Related Tags (New Search): Safety and performance,   Recalls,   Veterinary medicine

Guidelines for Recall/Withdrawal of Medicines (MCC: 5.07, Dec 2008)

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

Guidelines for Recall/Withdrawal of Medicines, Medical Devices and IVDs (MCC: 5.07, Nov 2015)

This is a draft guideline incorporating medical devices. Not yet finalised

Related Tags (New Search): GMP,   QMS,   IVDs,   Non-compliance,   Recall,   Recalls,   Safety,   Adverse Drug Reaction,   SRPINS,   Adverse Drug Event