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Iso 13485 Medical Device Articles & Analysis
5 articles found
Quality issues in medical devices often point to underlying weaknesses in the system, and ISO 13485-compliant CAPA is essential for correctly identifying cause and preventing the problem from recurring. Here’s an overview of CAPA requirements in ISO 13485 for medical ...
Food & Drug Administration (FDA) quotes the International Medical Device Regulatory Forum’s definition: "software intended to be used for one or more medical purposes that perform these purposes without being part of a hardware medical device." ...
It is an undeniable fact that safety and quality are the top-most priority for medical device companies. However, the best-practices to maintain these priorities are defined under ISO 13485. ...
” With this philosophy in mind, the UK-based business has released two devices that specifically cater for the medical market with safety practices for patients and health professions at the heart of their design – the G200 and G210 gas detectors. ...
” With this philosophy in mind, the UK-based business has released two devices that specifically cater for the medical market with safety practices for patients and health professions at the heart of their design – the G200 and G210 gas detectors. ...