Inspection

The consequence of a stray label or an IFU could be the cause of a product recall, so manufacturers need to take precautions to avoid this as manual or weak processes could put the process in jeopardy.

By applying predictive analytics, medical device companies can make a shift to a proactive mode to avoid potential problems before they happen, according to an expert in business strategy and software engineering.

A look at how one medical device manufacturer automated quality management along with ideas on how shared intelligence can drive quality from the shop floor to the top floor.

Here are some takeaways from ISO 19227 for orthopedic implants.