NAIONALNY KLASYFIKATOR UKRAINY EDYNYY ZAKUPIVEL'YI SLOVNIK DK 021:2015: 85140000-2 - Services in the field of health care (various) (MYD88 (L265P) mutation; Mutation analysis, deletions, insertions in the CALR gene; Mutation analysis, deletions in the MPL gene; Diagnosis of myeloid disorders (cytomorphological examination, immunophenotyping, confirmation of clonality); Determination of minimal residual disease (cytomorphological remission, flow cytometry for primary phenotype presence); Diagnosis of nocturnal hemoglobinuria and related disorders (PNH clone detection); Diagnosis of acute B-lymphoblastic leukemia: translocations t(9;22)(q34.1;q11.2) BCR::ABL1, t(12;21)(p13;q22) ETV6::RUNX1, 11q23 KMT2A (MLL) (FISH); Diagnosis of acute myeloblastic leukemia: translocations t(8;21) RUNX1::RUNX1T1, inv(16)(p11q22)/t(16;16) CBFB::MYH11, 11q23 KMT2A (MLL), t(15;17) PML::RARA, t(9;22) BCR::ABL1 (FISH); Diagnosis of acute myeloblastic leukemia (max): translocations t(8;21) RUNX1::RUNX1T1, 16q22.1 CBFB, 11q23 KMT2A (MLL), t(15;17) PML::RARA, t(9;22) BCR::ABL1, inv(3) (q21q26.2), t(3;3) (q21q26.2) GATA2::MECOM, 9q34 (NUP214) (FISH); Diagnosis of myelodysplastic syndrome (FISH). Deletion 5q, 7q; Diagnosis of myeloid disorders: translocations t(14;20) MAFB::IGH, t(14;16) MAF::IGH, t(4;14) FGFR3::IGH, t(11;14) CCND1::IGH, deletion 13q14, deletion 17p13.1 (TP53), 1q21, 1p32) (FISH); Bone marrow trephine biopsy (including necessary histochemical stains for pathological selection); Diagnostic immunohistochemistry 3 complexity categories (determination of histological type of undifferentiated malignant tumors, lympho- and myeloproliferative pathologies (lymphadenopathy, Hodgkin's lymphomas and non-Hodgkin's lymphomas, skin lymphomas, plasma cell neoplasms, mastocytosis, histiocytoses, myeloproliferative disorders); 'Philadelphia chromosome' t(9;22) (q34.1;q11.2) BCR/ABL1 (FISH); Investigation of surrogate markers of mutation status in the variable region of heavy chain immunoglobulin genes (IgVH genes); Investigation of bone marrow and blood products for hemoblastosis (cytomorphological and cytochemical methods); Deletion 17p13.1 (TP53) (FISH); Direct Coombs test; Erythropoietin; Diagnosis of lymphoproliferative disorders (cytomorphological examination, immunophenotyping); Diagnosis of acute leukemias (cytomorphology, cytochemical examination, FAB variant, immunophenotyping); Serum iron binding capacity; Folic acid; Transferrin; Determination of cyclosporin concentration in blood; Mutation analysis in the FLT3 gene)

The MUNICIPAL NON-PROFIT ENTERPRISE "VINNYTSIA REGIONAL CLINICAL HOSPITAL IM. M.I. PYROGHVA VINNYTSIA REGIONAL COUNCIL" in Ukraine from Europe region has released this tender for NAIONALNY KLASYFIKATOR UKRAINY EDYNYY ZAKUPIVEL'YI SLOVNIK DK 021:2015: 85140000-2 - Services in the field of health care (various) (MYD88 (L265P) mutation; Mutation analysis, deletions, insertions in the CALR gene; Mutation analysis, deletions in the MPL gene; Diagnosis of myeloid disorders (cytomorphological examination, immunophenotyping, confirmation of clonality); Determination of minimal residual disease (cytomorphological remission, flow cytometry for primary phenotype presence); Diagnosis of nocturnal hemoglobinuria and related disorders (PNH clone detection); Diagnosis of acute B-lymphoblastic leukemia: translocations t(9;22)(q34.1;q11.2) BCR::ABL1, t(12;21)(p13;q22) ETV6::RUNX1, 11q23 KMT2A (MLL) (FISH); Diagnosis of acute myeloblastic leukemia: translocations t(8;21) RUNX1::RUNX1T1, inv(16)(p11q22)/t(16;16) CBFB::MYH11, 11q23 KMT2A (MLL), t(15;17) PML::RARA, t(9;22) BCR::ABL1 (FISH); Diagnosis of acute myeloblastic leukemia (max): translocations t(8;21) RUNX1::RUNX1T1, 16q22.1 CBFB, 11q23 KMT2A (MLL), t(15;17) PML::RARA, t(9;22) BCR::ABL1, inv(3) (q21q26.2), t(3;3) (q21q26.2) GATA2::MECOM, 9q34 (NUP214) (FISH); Diagnosis of myelodysplastic syndrome (FISH). Deletion 5q, 7q; Diagnosis of myeloid disorders: translocations t(14;20) MAFB::IGH, t(14;16) MAF::IGH, t(4;14) FGFR3::IGH, t(11;14) CCND1::IGH, deletion 13q14, deletion 17p13.1 (TP53), 1q21, 1p32) (FISH); Bone marrow trephine biopsy (including necessary histochemical stains for pathological selection); Diagnostic immunohistochemistry 3 complexity categories (determination of histological type of undifferentiated malignant tumors, lympho- and myeloproliferative pathologies (lymphadenopathy, Hodgkin's lymphomas and non-Hodgkin's lymphomas, skin lymphomas, plasma cell neoplasms, mastocytosis, histiocytoses, myeloproliferative disorders); 'Philadelphia chromosome' t(9;22) (q34.1;q11.2) BCR/ABL1 (FISH); Investigation of surrogate markers of mutation status in the variable region of heavy chain immunoglobulin genes (IgVH genes); Investigation of bone marrow and blood products for hemoblastosis (cytomorphological and cytochemical methods); Deletion 17p13.1 (TP53) (FISH); Direct Coombs test; Erythropoietin; Diagnosis of lymphoproliferative disorders (cytomorphological examination, immunophenotyping); Diagnosis of acute leukemias (cytomorphology, cytochemical examination, FAB variant, immunophenotyping); Serum iron binding capacity; Folic acid; Transferrin; Determination of cyclosporin concentration in blood; Mutation analysis in the FLT3 gene) with tender notice no. UA-2026-10-29-012515-a published on 30 Oct 2026. The tender is due to expire on 14 Nov 2026. This tender is sourced from Ukraine Procurement Platform and is eligible for suppliers interested in Blood-testing reagents, Laboratory services, Blood analysis services, Diagnostic test, Molecular diagnostic. Interested bidders can obtain further information including complete bid documents or ways to participate by registering on Tender Impulse and referencing via Tender Impulse ID 16048616.