Leveraging Traceability in Medical Device Development

Innovation in the medical device development industry is hampered by complex standards and regulations and once the medical device prototype is developed and tested, it then faces a long approval process. In the development and servicing of medical devices, complete traceability is one of the most important requisites to compliance with relevant ISO/IEC/FDA standards. This article from Intland describes why traceability is essential for ensuring the compliance with medical device standards and regulations.

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Find out how T&VS Medical Testing services help ensure and conveniently prove traceability, and satisfy requirements of various medical industry standards.

2016-04-20T06:36:24+00:0020th April, 2016|Blog, Thought Leadership|