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the Health Sciences authority or HSE as a post market surveillance program to monitor the quality safety and efficacy of their building products in Singapore one component of this program is the management of product defects as the product registrant manufacturer importer or supply of therapeutic product you are required to do the following to report product defects related to your therapeutic product to HSA or to notify us if you are recalling any product before initiating the recall process this video aims to provide you with information regarding the requirements and the processes for further defect reporting and product recalls further defects can arise during the manufacturing the storage and the handling of therapeutic products it is important that you report these defects arising from during these processes especially if they can affect a product safety quality and efficacy this can help identify issues that may affect the users and ensure measures are taken to protect public he