ISO 13485 is the ISO standard that specifies requirements for a comprehensive quality management system for manufacturers of medical devices. ISO 13485:2016 was published by ISO on January 1, 2016. Any firm involved in the design, production, installation, or servicing of medical equipment can benefit from ISO 13485 training courses to better understand and apply quality management requirements.
https://ias-certification.com/....iso-13485-training-i
AS9100 is an international quality management system standard specifically created for the aerospace industry. It was developed by the International Aerospace Quality Group (IAQG) in conjunction with leading aerospace organizations worldwide and is based on ISO 9001:2015.
https://ias-certification.com/....as-9100-certificatio
AS9100 is an international quality management system standard specifically created for the aerospace industry. It was developed by the International Aerospace Quality Group (IAQG) in conjunction with leading aerospace organizations worldwide and is based on ISO 9001:2015.
https://ias-certification.com/....as-9100-certificatio
ISO 13485 is a crucial international standard designed to enhance the quality management systems of organizations involved in manufacturing medical devices and equipment. This certification outlines stringent control measures to minimize operational errors in the manufacturing process and emphasizes continual improvement in the quality of medical equipment.
https://ias-certification.com/....iso-13485-certificat
CE stands for “ConformiteEuropene,” which translates to “European Conformity.” This mark is required for products to be accepted into the European business market. CE certification ensures that the product and its packaging comply with European safety and quality standards.
https://ias-certification.com/....ca/ce-marking-certif
