This tender with title Закупка Финголимода (торговое наименование "Гилениа") для лечения больных гемофилией, муковисцидозом, гипофизарным нанизмом, болезнью Гоше, злокачественными новообразованиями лимфоидной, кроветворной и родственных им тканей, рассеянным склерозом, гемолитико-уремическим синдромом, юношеским артритом с системным началом, мукополисахаридозом I, II и VI типов, апластической анемиейнеуточненной, наследственным дефицитом факторов II (фибриногена), VII (лабильного), X (Стюарта-Прауэра), а также после трансплантации органов и (или) тканей -- Purchase of Fingolimod (trade name "Gilenia") for the treatment of patients with hemophilia, cystic fibrosis, pituitary dwarfism, Gaucher disease, malignant neoplasms of lymphoid, hematopoietic and related tissues, multiple sclerosis, hemolytic uremic syndrome, juvenile arthritis with systemic onset, mucopolysaccharidosis I, II and VI types, unspecified aplastic anemia, hereditary deficiency of factors II (fibrinogen), VII (labile), X (Stuart-Prauer), as well as after organ and (or) tissue transplantation has been published on Bidding Source portal dated 20 Jan 2022 for the country of Russia. It has been categorized on Planting and maintenance services of green areas & Pituitary, hypothalamic hormones and analogues. For similar tenders you can see tenders mentioned below of this page.
Purchase of Fingolimod (trade name "Gilenia") for the treatment of patients with hemophilia, cystic fibrosis, pituitary dwarfism, Gaucher disease, malignant neoplasms of lymphoid, hematopoietic and related tissues, multiple sclerosis, hemolytic uremic syndrome, juvenile arthritis with systemic onset, mucopolysaccharidosis I, II and VI types, unspecified aplastic anemia, hereditary deficiency of factors II (fibrinogen), VII (labile), X (Stuart-Prauer), as well as after organ and (or) tissue transplantation
General Information
Purchase of Fingolimod (trade name "Gilenia") for the treatment of patients with hemophilia, cystic fibrosis, pituitary dwarfism, Gaucher disease, malignant neoplasms of lymphoid, hematopoietic and related tissues, multiple sclerosis, hemolytic uremic syndrome, juvenile arthritis with systemic onset, mucopolysaccharidosis I, II and VI types, unspecified aplastic anemia, hereditary deficiency of factors II (fibrinogen), VII (labile), X (Stuart-Prauer), as well as after organ and (or) tissue transplantation
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