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.