It is well known in the medical device industry that the success of a company is driven by its ability to bring innovative, cost-effective products to market quickly. And, in today’s global medical device market, proactive strategies are needed to ensure compliance with the regulatory requirements in global markets. As the Food and Drug Administration (FDA) and other regulatory bodies have embraced the concept of total product life cycle (TPLC) management, it has become the gold standard for guiding a medical device from concept to completion.

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