FDA’s Five Year Plan: Better Documentation - Level 3 Inspection

FDA’s Five Year Plan: Better Documentation

The FDA recently unveiled its Strategic Priorities 2011-2015.
How will the next five years’ goals and objectives affect you?
“If it isn’t documented, it didn’t happen” is one of the FDA’s best-known unwritten rules.  As the agency’s resources are already stretched thin, the medical device industry is being held to an ever-higher standard of data collection.

With accurate and comprehensive computer-aided inspection (CAI) you can satisfy regulators by recording and documenting every surface data point and every extracted dimension for future reference — while cutting iterations, months, and millions of dollars from the process development schedule.  The same can hardly be said for fixed gauges or optical-comparator overlays!

Visit www.level3inspection.com or call us today to learn more!

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