Global Medical Device Podcast powered by Greenlight Guru cover image

Common QMS Mistakes SaMD Companies Make

Global Medical Device Podcast powered by Greenlight Guru

CHAPTER

How Does That Fit Into Your Quality Management System?

You've got things like non performing products, for example, in ISO 13485. There's a different procedure of when the defective product is noticed or the non performing product before delivery or after delivery with the software that's not really applicable. The other thing that I mentioned is your handling property. And again, if you have physical components, again, this often is modifiable or depending on the customer requirements. So how are you going to store the defective product away from the actual product that works?"

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