![]() ![]() It also covers aspects such as storage, distribution, installation and servicing, servici ng, and the provision o associated services. It is designed to be used by organizations throughout the lie cycle o a medical device, rom initial conception to production and post-production, including final decommission and disposal. ISO ����� ISO �����, Medical devices – Quality management systems – Requiremen Requirementts for regulatory regulatory purposes purposes, is an internationally agreed standard that sets out the requiremen requirements ts for a qualit qualityy management system specific to the medical devices industry. ![]() ISO ����� Quality management for medical devices
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