240 likes | 465 Views
ISO 13485:2016 is a Quality Management System standard for Medical Devices, has been harmonized with European Medical Devices Directives i.e MDD, AIMDD and IVDD. EN ISO 13485:2012 is now updated as ISO 13485:2016, in the EU Official Journal, with the date of u2018cessation of presumption of conformityu2019 of EN ISO 13485:2012 stated as 31 March 2019.<br><br>
E N D
ISO 13485 Certification ISO 13485 Certification is the commonly used certification to represent the Quality Management System of medical devices and equipment. This certification is applicable for all the organizations that manufacture/supply medical devices. It enhances the confidence of the consumers in your products and services. Moreover, the ISO 13485 Certification demonstrates the effective implementation of the medical devices and equipment. About ISO 13485 Standard ISO 13485 is also one of the Quality Management System standards so you can easily implement it in your organizations. It has similar requirements as ISO 9001 and also includes its additional requirements. Both the standards are focused only in the development of high- quality products. But the major difference is, the ISO 9001 ensures customer satisfaction with quality products and services whereas the ISO 13485 standard includes requirements to improve the quality of medical devices and equipment. The ISO 13485 standard provides guidelines for the manufacturers to improve the quality of medical devices from the manufacturing process, installation to servicing process. Also, it ensures the medical devices are safe and are made for their intended purpose.