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Ten tips for a successful ISO/IEC 27001 audit
- July 10, 2024
- Posted by: Anita Tullari
- Category: Quality, Environment, Health and Safety & Sustainability
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An ISO/IEC 27001 audit verifies if your organization’s management system complies with standards and assesses the adequacy of risk management measures.An ISO/IEC 27001 audit verifies if your organization’s management system complies with standards and assesses the adequacy of risk management measures.
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ISO 13485:2016 – 5 Frequent Errors and How to Address
- January 24, 2024
- Posted by: MSECB Marketing
- Category: Quality, Environment, Health and Safety & Sustainability
Explore ISO 13485:2016 challenges through the expertise of Danny Kroo. Learn about common misinterpretations for improved quality management.
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The rising importance of Quality in the Medical Device Industry
- November 23, 2021
- Posted by: Hana Maxhuni
- Category: Quality, Environment, Health and Safety & Sustainability
The medical devices Quality Management System, commonly known as ISO 13485:2016, is the reference standard for the Medical Devices industry, developed and published as the third edition by International Organization for Standardization (ISO).
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COVID-19 increases the need for new medical devices
- November 23, 2021
- Posted by: Hana Maxhuni
- Category: Quality, Environment, Health and Safety & Sustainability
This article presents an overview of the challenges that accompany the design and development of Medical Devices in accordance with the legal and regulatory laws and ISO management system standards.
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ISO 13485 – Q&A Session
- November 22, 2021
- Posted by: Hana Maxhuni
- Category: Quality, Environment, Health and Safety & Sustainability
This session covers the most frequently asked questions about the ISO 13485:2016 standard. ISO 13485 is designed to be used by any organization that is involved in the design, production, installation and servicing of medical devices and related services.
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