Make Sure You Don't Have the Most Common Problems that IVD Manufacturers Make Before Your Next Audit!

As a Notified Body that offers CE Marking for IVDs, LNE/G-MED works every day with IVD manufacturers to assess their quality system according to the European Directive.

Our IVD Specialist and Project Manager reviewed our IVD files and found the four most common mistakes that IVD manufacturers make.  While none of the mistakes were serious, most were caused by simple oversights or a misunderstanding of the Directive’s intent.  

Make sure you correct these mistakes, oversights, and understandings before they become nonconformities.  Save time and hassle by fixing them now, before your next audit!  LNE/G-MED compiled the top nonconformities into this free report.  Just complete the form below to receive this report via email.