This tender with title Закупка Интерферона бета-1а (торговое наименование Ребиф) 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 Interferon beta-1a (trade name Rebif) 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 a 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 08 Feb 2022 for the country of Russia. It has been categorized on Pituitary, hypothalamic hormones and analogues & Planting and maintenance services of green areas. For similar tenders you can see tenders mentioned below of this page.
Purchase of Interferon beta-1a (trade name Rebif) 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 a 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 Interferon beta-1a (trade name Rebif) 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 a 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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