CERTIFICAZIONE ISO 27001
La certificazione ISO 27001 è un riconoscimento formale della conformità di un’organizzazione ai criteri ISO 27001:2013. Le organizzazioni che vogliono rafforzare il proprio sistema di gestione della sicurezza delle informazioni (ISMS) richiedono solitamente la certificazione ISO 27001.
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ISO 9001 CERTIFICATION
Firstly, the ISO 9001 Certification is the most popular certification, followed by millions of organizations throughout the world. This ISO Quality Management System Certification helps the organization to bring effective improvements in communication, production, manufacturing process, and services. It also enhances the quality management system performance in all phases of the organization. It improves customers’ satisfaction as well as stakeholders’ confidence. This helps you have a sturdy and long-lasting relationship with your business partners.
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CE MARKING CERTIFICATION
CE Marking Certification is a must to declare that your product and its packaging are made in compliance with European safety, quality, and environmental protection standards. This European conformity certification is essential to selling your product in the European Economic Area (EEA). It enhances credibility as well as the customers’ satisfaction in your products. It promotes your brand image and also helps you attain more customers. Moreover, the CE Marking Certification improves the marketability of your product and increases the profitability of your business.
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ISO 27001 CERTIFICATION
Similar to other management systems, 27001 is based on the P-D-C-A approach towards quality improvement. ISO 27001 certification for IT companies offers a methodological and well-organized attitude that will protect the confidentiality of your data, fortify the integrity of business data, and intensify the availability of your business IT systems.
https://iasiso-gulf.com/iso-27....001-certification-in

ISO 13485 CERTIFICATION
ISO 13485 is a standard specifically developed by ISO (International Organization for Standardization) for medical devices and equipment. This international standard specifies the requirements to improve the performance of the Quality Management System to consistently deliver quality medical devices and related services. It helps organizations to comply with customers and also with applicable regulatory requirements. Furthermore, the requirements of ISO 13485 not only apply to medical devices and equipment, but also apply equally to the associated services provided by the organization.
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