How Is The FDA Doing On Medical Device Review Times?

In 2012, following years of concern over U.S. Food and Drug Administration (FDA) medical device review processes that were viewed as increasingly unpredictable and inefficient, plaguing investment, innovation and U.S. competitiveness, stakeholders including Congress, the Agency and the medical device industry worked to identify potential solutions. The shared goal: to improve product review times while also maintaining rigorous scientific and patient safety standards.

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