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Manufacturers of medical devices are required to adhere to a quality management system (QMS) that complies with ISO 13485:2016 because medical devices require a high level of reliability and safety. ISO 50001:2018 is a standard for energy management systems (EnMS) that can be used in manufacturing facilities for medical devices to help cut down on energy use and make them more sustainable. Manufacturers of medical devices can identify areas for improvement in energy efficiency, establish targets for improvement, implement energy-saving measures, and continuously improve energy performance over time by implementing ISO 50001:2018. Additionally, this may assist manufacturers in enhancing their reputation, cutting costs, and adhering to regulatory requirements
An international standard known as ISO 50001 aids businesses in lowering their energy consumption and costs. It was first published in 2011 and was updated in 2018 to reflect industry shifts in energy management. New sections on energy performance indicators and energy baselines are included in the standard, which places an emphasis on the role that top management plays in driving improvements to energy performance. It is made to work with other ISO management system standards, making it easier to manage energy efficiently. In general, ISO 50001 helps the world fight climate change and cut greenhouse gas emissions
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