![]() It can be purchased from the ISO website for its international version, or from a national standardization organization (e.g. The current version of the standard is ISO 13485:2016, Medical devices – Quality management systems – Requirements for regulatory purposes. ISO 13485 is meant to help medical device companies (primarily medical device manufacturers) set up a QMS that demonstrates consistent design, development, production, storage, distribution, installation, servicing, final decommissioning, and/or disposal of medical devices, as well as design and development, or provision of associated activities (e.g. Conversely, ISO 9001 is not required to support medical device regulatory approval in any country. This standard is based on the internationally recognized ISO 9001 QMS standard (which is not specific to any industry or type of product) and incorporates additional elements relevant to medical device processes.Īlthough ISO 13485 only covers QMS requirements and does not define medical device quality, some countries require ISO 13485 certification to support medical device regulatory approval. ![]() ISO 13485 is a stand-alone standard published by the International Organization for Standardization (ISO) that provides requirements for quality management systems (QMS) of companies involved in the medical device industry. What is the relationship between ISO 13485 and MDSAP?. ![]() ![]() What countries require ISO 13485 certification?.Who needs QMS certification under ISO 13485?.What is a Quality Management System (QMS)?. ![]()
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