ISO 13485 Internal Auditor Training outlines quality management system requirements for design, development, production, and servicing of medical devices and related services. The purpose of ISO 13485 Internal Auditor Training is to provide personnel with the necessary knowledge to plan and conduct an audit of a medical device company in accordance with ISO 13485 Internal Auditor Training standard. ISO 13485 Internal Auditor Training also provides information for the development of an audit program.

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ISO 13485:2016 is the most recent version of the ISO 13485 standard, which was developed with a process-oriented approach in mind to reduce operational errors and hazards in the management system. Because it is presented with a high-level framework and PDCA cycle, ISO 13485:2016 is compatible with other ISO management system standards. Furthermore, its risk-based thinking style helps businesses to satisfy the demands of their customers on a continuous basis.

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ISO 50001 is an international standard for energy management. It provides a framework for organizations to demonstrate their commitment to the sustainable use of energy and contribute towards mitigating its adverse impacts on society and the environment. ISO 50001 also helps organizations save money through more efficient energy usage. ISO 50001 was created by the International Organization for Standardization (ISO). ISO is a non-governmental organization with a membership of over 162 national standards bodies.
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O treinamento ISO é realizado em vários níveis e estágios. Com a vasta experiência em auditoria no campo da ISO, a IAS lida com todo tipo de treinamento em ISO de uma maneira abrangente, como Treinamento de Auditor Líder ISO, Treinamento de Auditor Interno ISO, Conscientização ISO e Treinamento Básico.
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Enhance the knowledge and skills to perform a full audit by taking advance ISO 9001 training called ISO 9001 Lead Auditor Course. This IRCA accredited ISO 9001 lead auditor training guides the delegates with ISO 9001 requirements and principles of QMS to plan, conduct, and manage both internal and as well as external audits of QMS.
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