Usability report at M18

This report will integrate all the User Interface Specifications by design per each product as well as will act as a validation report to ensure the applicability and the validity of the design of the four IVD medical devices as per EN 623662008 requirements The updated report should be performed based on the design changes for the industrial manufacturing scaling up and should accompany the submission of the relevant Technical Documentation of the fours products to the selected Notified Body