Background The bioequivalence of Concor (R) (Merck Healthcare KGaA, Darmstadt, Germany), a bisoprolol-containing tablet, manufactured in China and Concor (R) tablets manufactured in Germany has not been previously reported.Methods This single-center, open-label, randomized, two-period, two-sequence, crossover trial (28 February 2023-19 May 2023) compared the pharmacokinetics and safety of bisoprolol 5-mg tablets manufactured in China (test product) with those of bisoprolol 5-mg tablets manufactured in Germany (reference product) in healthy Chinese adults under fasted and fed conditions. Primary endpoints were Cmax, AUC0-tlast, and AUC0- infinity .Result The mean (coefficient of variation percentage) Cmax in the fasted group was 21.2 (15.0) ng/mL (test product) and 22.1 (17.0) ng/mL (reference product). Under fed conditions, the respective Cmax values were 22.7 (18.8) ng/mL and 22.8 (15.2) ng/mL. The mean and coefficient of variation percentage for AUC were also similar between the two products. The geometric least squares mean ratio (90% confidence interval) for the test/reference product was 0.9565 (0.9006-1.0158) ng/mL for Cmax, 0.9761 (0.9370-1.0168) h<middle dot>ng/mL for AUC0-tlast, and 0.9807 (0.9429-1.0200) h<middle dot>ng/mL for AUC0- infinity in fasted conditions and 0.9966 (0.9289-1.0691) ng/mL for Cmax, 0.9672 (0.9220-1.0145) h<middle dot>ng/mL for AUC0-tlast, and 0.9693 (0.9253-1.0155) h<middle dot>ng/mL for AUC0- infinity in fed conditions, which met the pre-defined criteria for bioequivalence. No serious treatment-emergent adverse events or deaths were observed.Conclusion This study compared the bioequivalence of bisoprolol 5-mg tablets manufactured in China to that of the tablets manufactured in Germany among healthy Chinese adults.Systematic Review Registration identifier CTR20230391