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The Health Sciences Authority (HSA) in Singapore oversees a post-market surveillance program to ensure the quality, safety, and efficacy of therapeutic products. A key aspect of this program is managing product defects. As a registrant, manufacturer, importer, or supplier, you must report any product defects to HSA and notify them if you are recalling a product. This video provides essential information on the requirements and processes for defect reporting and recalls. Defects can occur during manufacturing, storage, and handling, so it is crucial to report these issues, particularly if they impact product safety, quality, or efficacy. Timely reporting helps identify risks to users and implement protective measures for public health.