The International Standardization Organization’s Technical Management Board is looking to rewrite the standard for ISO 13485, despite the fact that medical device manufacturers are not required to adopt the most recent version of the standard until March of 2019. In response, the ISO Technical Committee 210 has devised a survey for industry device makers and other stakeholders, with the aim of determining the impact that a rewrite of the standard would have. Take a deeper look at the issue in this Medtech Insight article.
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices Training Course (March 13, 2025)
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