The medical device industry is coming under increased scrutiny for their manufacturing processes. Medical device product recalls are becoming more common, and this is putting the entire industry under a microscope. You may have your own thoughts on the matter, but there are some clear-cut ways to show that you are doing things correctly when it comes to quality systems. ISO 13485 is a standard which applies to medical device manufacturers worldwide, covering all stages in the manufacturing process from design and development. This blog will provide more information on ISO 13485 and its requirements.