Because freesia is a crop that is typically vegetatively propagated from offsets, a degradation in its genetic character or an onset of after successive culturing over a long period. To produce virus-free freesia corms, apical meristem culture and rapid mass propagation must be established. This study aimed to establish the rapid mass production of in vitro freesia corms using a bioreactor. Shoots (12 – 15 cm in height) obtained from tissue culture were used as the plant material in a balloon-type bubble bioreactor in which medium strength, sucrose concentration, inoculation plant volume, and medium exchange method were determined. Medium strengths tested included full strength (1), 1/2, and 1/4 strength MS medium; sucrose concentration 9% 12%, and 15%, and inoculation plant volumes were tested at 40, 80, 120, and 160 shoots/1L medium. MS medium was supplemented with a 1/2 volume of the initial volume or the medium was completely exchanged with a new medium or not exchanged at all throughout the experiment. Results indicated the best growth of freesia corms at 1/2 strength medium, 9% sucrose, 120 shoots/L medium, with complete medium exchange 4 weeks after initiating the experiment. Under these culturing conditions, corms with 0.5 g fresh weight, 0.15 g d ry w eight, 1 3 mm h eight, a nd 0 .9 mm diaeter were harvested from the bioreactor within only 6 weeks, which were large enough to be planted in field. Thus, our results indicated that the cost and period for the production of freesia corms in vitro can be markedly decreased.