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A protocol was developed for plant regeneration of Melia azedarach L. by in vitro culture of apical meristem (0.5 mm in length). The influence of six clones was investigated. The culture procedure comprised two sequential steps: 1) Induction of shoots by in vitro culture of axillary buds from adult trees (10-15 years old) by culture on Murashige and Skoog3(1962) medium (MS) supplemented with 0.5 mg.dm-BAP (6-benzylaminopurine), 0.1 mg.dm -3 IBA (indolebutyric acid), and 0.1 mg.dm -3 GA3 (gibberellic acid). The Multiplication of the regenerated shoots was achieved in MS + 0.5 rag.din -3 BAP + 0.1 mg.dm -3 GA3.2) In vitro culture of the apical meristems from the regenerated shoots in MS medium (0.7 %) supplemented with various combinations of BAP and IBA.Maximum shoot proliferation was obtained on MS medium supplemented with 0.5 mg-dm -3 BAP and 0.1 mg.dm 3 IBA.Regenerated shoots were rooted on MS + 3.5 mg.dm -3 IBA (4 days) followed by subculture on MS lacking growth regulators (30 days). Complete plants were transferred to soil.