Automation continues to transform medical device manufacturing, helping organizations improve quality, consistency, and production efficiency. But implementing automation in a highly regulated environment requires more than just advanced equipment—it also demands rigorous validation and qualification processes to ensure compliance without slowing innovation.

In this Videobites interview, Phil Burn, Manufacturing Engineering Manager at MRPC, explains how the right automation strategy can balance speed, quality, and regulatory requirements. He also discusses how qualification activities such as IQ, OQ, and PQ play a critical role in bringing automated systems online while enabling manufacturers to increase production capacity and scale alongside growing customer demand.

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