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Why Automation Is Becoming a Regulatory Expectation in Medical Device Manufacturing In the past, automation in medical device manufacturing was often viewed as a productivity enhancement. Today, regulators increasingly see it as essential. They're not just asking for documented procedures, they’re looking for evidence of quality built into the system itself. Automation is emerging as the clearest way to demonstrate that. 1. Manual Processes Still Introduce Variability Even we

Update on the regulatory landscape

A look at how much time and money you could save by automating your processes.

This post explains what poka-yoke is and why it is important in biotech. Poka-Yoke refers to designing processes that make errors unlikely or impossible.