“…The method consists of four main steps: (a) the injection of the fibrin components including the cells into the silicone tube, (b) the gelation process, (c) the ejection of the gel after polymerization and (d) the stretching of the resulting fiber. We expect that already existing solutions for automated pipetting, handling, collection, gripping of samples and controlled linear displacement could be assembled to create an ad‐hoc automated system for the production of the fibers in a sterile, closed environment (Bhuthalingam, Lim, Irvine, & Venkatraman, ; Bartolo, Domingos, Gloria, & Ciurana, ; P. F. Costa et al, ; Kikuchi et al, ; Mekhileri et al, ). A GMP conform production is facilitated by the limited number of parts in contact with the materials composing the fibers and the commercial availability of GMP‐conform cell‐work stations.…”