Three experiments were carried out with the aim of evaluating the efficiency of techniques of in vivo production, storage and transfer of embryos in dairy sheep. Experiment I -For embryo production, thirty-one ewes were synchronized with FGA (vaginal sponges, 40 mg, 9 d) and PGF2α (ICI; 50 µg, 7 th d), and subdivided into three groups corresponding to the following superovulatory treatments over 3 days with purified gonadotrophic preparations: A) control, FSH/LH ratio = 1 (250 IU p-FSH : 250 UI p-LH); B) FSH/LH ratio = 2 (250 IU p-FSH : 125 IU p-LH) and daily FSH/LH ratio of 3.4 -1.7 -0.8 in the 3 days of treatment, respectively; C) FSH/LH ratio = 2 (250 IU p-FSH : 125 IU p-LH) and daily FSH/LH ratio of 5.0 -1.0 -0.3. On the 7 th day after oestrus and mating, ovarian response and embryo production were evaluated. Experiment II -Three freezing methods were evaluated based upon post-thaw embryo quality: CF) conventional slow freezing by 1.5 M ethylene glycol (EG); V-1) one-step vitrification based on exposure of the embryos to one solution (EG 7.15 M + ficoll 2.5 mM); V-3) vitrification in three steps, corresponding to three solutions at increasing concentration of glycerol (GLY) and EG (GLY 1.4 M; GLY 3.4 M + EG 1.4 M; GLY 4.6 M + EG 3.4 M). V-1) and V-3) frozen embryos were directly plunged in liquid nitrogen. At thawing, embryo viability was evaluated on the basis of morphological features. Experiment III -For embryo transfer, a total of 26 recipient ewes were synchronized with donors. On the 7 th d from oestrus, 11 recipient ewes received fresh embryos (Group FE -control) and 15 recipients received vitrified-thawed embryos (Group VTE). Each recipient received 2 embryos. Superovulatory treatment B) significantly advanced the onset of oestrus compared to the control (27.3 vs 34.7 h; P<0.05). Ovulation rate did not differ among the groups (6.5 to 10.8). Transferable embryos in Group B) (7.2) resulted similar to Group A) (5.3) and significantly (P<0.05) different when compared to Group C) (3.2). V3-method resulted in the highest (P<0.01) transferable embryos (74.5%) compared to CF-and V1-methods. After transfer, in FE and VTE recipient ewes were comparable in fertility rates (72.7 vs 73.3%; P>0.05) and embryo survival (63.6 vs 56.7%; P>0.05). In conclusion, the results demonstrated that treatments B) and C) did not improve superovulatory response compared to A); for embryo cryopreservation the V3 method can successfully be used for embryo transfer in ewes. (27,3 vs 34,7 ore; P<0,05). Il tasso di ovulazione non è stato influenzato dal trattamento (6,5 -10,8; P>0,05). La produzione di embrioni trasferibili registrata nel Gruppo B) (7,2) è stata similare al controllo (Gruppo A, 5,3) e maggiore rispetto al trattamento C) (3,2; P<0,05