Medical device and health care software development teams are faced with increased product & software complexity, and increasingly stringent regulations. In such a highly regulated environment, finding an efficient way to ensure and prove compliance with relevant standards is vital.

This article from Intland describes how risk management is gaining more and more importance, and is increasingly becoming a fundamental requirement of the regulations and standards that apply to medical device development.

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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.