We previously demonstrated that dendritic cells (DC) that have endocytosed apoptotic bodies of autologous leukemic cells (Apo‐DC) can boost antileukemic T‐cell responses. In this study, we report a description of the production procedure and product specification of the Apo‐DC vaccine preparations for clinical use. Enriched populations of CD14+ monocytic precursors and CD19+ leukaemic cells were obtained using CliniMACS technology from a single leukapheresis product. Apoptotic bodies were obtained by irradiating (5 Gy) CD19+ selected B cells. DC were generated ex vivo by culturing monocytes with granulocyte macrophage colony‐stimulating factor and interleukin‐4. Following coculture with apoptotic bodies, DCs were matured with tumour necrosis factor‐α. The mean percentage of CD14+ cells in the peripheral blood as well as in the leukapheresis product of the patients (n = 10) was approximately 2% (range, 0.8–3.3). Immunomagnetic selection using the CD14 reagent yielded a CD14+ population that was 91 ± 2.2% (mean ± SEM) pure. Immunomagnetic selection of CD19 expressing cells yielded a population that was 100 ± 0.03% pure. Cell viability immediately after selection was 97% and 98% after 7 days of culture. The Apo‐DC cellular vaccine product showed a mature phenotype, with a high rate of endocytosis (84%) of apoptotic leukemic B‐cells. In conclusion, despite significant variability in the circulating monocyte frequency of the chronic lymphocytic leukaemia patients, our method permitted the production of a DC vaccine with high reproducibility and conforming with recommended quality standards.