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The Health Sciences Authority (HSA) in Singapore oversees a post-market surveillance program to monitor the quality, safety, and efficacy of therapeutic products. A key aspect of this program is the management of product defects. As a product registrant, manufacturer, importer, or supplier, you must report any product defects to HSA and notify them before initiating a recall. This video provides essential information about the requirements and processes for reporting defects and executing product recalls. Defects can occur during manufacturing, storage, or handling, and it is crucial to report them, particularly if they impact safety, quality, or efficacy, to protect public health.