In the present study, macromolecular design of homo and copolymers of lactide (LA) and £-caprolactone (CL) in different structures by the use of biocompatible catalysts and co-initiators were performed to satisfy a need of tailor-made bioassimilable polymeric structures without any hazardous metal contaminants for various medical applications. Linear and star shaped (di, tetra and hexa functional) poly(L-lactide) (PLLA) and poly(£--caprolactone) (PCL) homo/copolymers were synthesized by using bismuth(III)acetate (Bi(III)Ac) and creatinine as biosafe catalysts and ethylene glycol, pentaerythritol and myo-inositol as co-initiators.The effect of catalyst type on polymer properties was observed by differences in crystalline structure. Crystalline and amorphous linear and star shaped PLLAs were obtained by using Bi(III)Ac and creatinine as catalysts, respectively. The activity of creatinine was very low comparing to Bi(III)Ac and SnOct2 catalysts. The reactivity of LA monomer was found to be higher than that of CL monomer. The high molecular weight polymers having low PDI values were obtained by using Bi(III)Ac catalyst contary to creatinine catalyst. The decrease in glass transition temperatures and molecular weights of synthesized PLLA and PCL homo/copolymers were observed with the increase in amount of co-initiators due to the decrease in chain length and disruption of crystal formation.The cytotoxicity properties of the catalysts and synthesized linear and functional homo/co PLLAs and PCLs were carried out according to MTT assay. Cytotoxicity of Bi(III)Ac was found as lower than that of SnOct2. Creatinine and the synthesized polymers did not show any cytotoxic properties. The observation of no cytotoxic effect of creatinine catalyst results in the biosafe usage of creatinine catalyst instead of toxic SnOct2 for the synthesis of moderate or low molecular weight homo/co PLLAs and PCLs in bioapplications.