{"id":3569,"date":"2021-07-07T15:09:41","date_gmt":"2021-07-07T14:09:41","guid":{"rendered":"https:\/\/www.imsm.com\/south-africa\/?p=3569"},"modified":"2021-07-13T09:59:35","modified_gmt":"2021-07-13T08:59:35","slug":"sahpra-and-iso-13485-medical-devices-compliance-for-south-africa","status":"publish","type":"post","link":"https:\/\/www.imsm.com\/south-africa\/news\/sahpra-and-iso-13485-medical-devices-compliance-for-south-africa\/","title":{"rendered":"SAHPRA and ISO 13485: Medical Devices compliance for South Africa"},"content":{"rendered":"

Medical safety is of the utmost importance, with the safety process starting well before patient care. Medical devices are designed to improve health and save lives. Therefore, medical devices compliance is essential to the success of all parties. Regulatory bodies, like SAHPRA (South African Health Products Regulatory Authority), have strict requirements to ensure medical devices are created with quality products that are safe to use. “SAHPRA is an entity of the National Department of Health, created by the South African Government to ensure that the health and well-being of human and animal health is at its core.”<\/p>\n

Globally, one of the best ways to comply with these regulations is with the internationally acknowledged ISO 13485 Management System, a symbol of quality no matter what language.<\/p>\n

What are SAHPRA\u2019s guidelines for medical devices?<\/h3>\n

A valid SAHPRA (South African Health Products Regulatory Authority) medical device establishment licence is necessary for Medical Device companies operating in South Africa. There are three types of licences available for medical device companies:<\/p>\n