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ISO 13485 certification ensures that medical device manufacturers meet stringent quality and safety standards.
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In the dynamic landscape of global business, ensuring the highest standards of quality, safety, and environmental responsibility is paramount. This realization has led to the widespread adoption of ISO certifications as a way for companies to demonstrate their commitment to excellence. In Duba ...
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The objective of this certification is to reduce/prevent accidents, deaths, and injuries of people and loss or damage ...
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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 ‘cessation of presumption of confor ...
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ISO 50001 is an energy management system (EnMS) standard published by the International Organization for Standardization (ISO). It provides organizations with a framework to improve their energy efficiency, use resources more sustainably, and reduce their environmental impact ...