The objectives of this study were to develop systems for mass proliferation, rooting, and reestablishment of microcuttings of Helleborus orientalis and Aconitum uncinatum. Basal medium for H. orientalis contained 1/2 MS with 0.4 mg thiamine–HCl/liter, 0.5 mg pyridoxine–HCI/liter, 0.5 mg nicotinic acid/liter, 100 mg i-inositol/liter, 5 mg BA/liter, 2% sucrose, and 0.7% Phytagar. There was no effect of GA (1 mg–liter–1) or TDZ (0.1, 1 mg–liter–1) on axillary shoot proliferation. Helleborus orientalis rooted in vermiculite, Redi-Earth, or 4 perlite: 1 peat with 50% to 56% survival. A field plot containing 18 clonal H. orientalis has been established. Basal medium for A. uncinatum contained WPM with 2% sucrose, 2.5 mg BA/liter, 150 ppm ascorbic acid, 150 ppm citric acid, and 0.7% Phytagar. There was no effect of photoperiod (8, 12, 14 h, 52.5 μmol–m–2–s–1 photosynthetic active radiation) or banana extract on axillary shoot proliferation. Significantly more axillary shoots were generated in the presence of BA (10 mg–liter–1) + kinetin (10 mg–liter–1). Medium containing 500 ppm of PVPP resolved blackening of microcutting bases. More than 500 in vitro-rooted microcuttings (1 mg IBA/liter) survived and grew when transplanted into MetroMix 510 and placed under humidity domes for 6 weeks in the mist.