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                     <efbc:ChangeDescription languageID="SLK"><![CDATA[Úprava znenia na základe otázky/námietky:
Vzhľadom k tomu, že kupujúci je subjektom verejného práva (podľa § 261 ods. 3 písm. d) a § 261 ods. 4 písm. a), b) Obchodného zákonníka) a zároveň poskytovateľom zdravotnej starostlivosti, zmluvné strany sa výslovne dohodli, podľa § 340b ods. 1 a 5 Obchodného zákonníka, že kupujúci je ako dlžník povinný plniť svoje  peňažné záväzky z dodania tovaru v lehote splatnosti 60 dní odo dňa doručenia faktúry; predávajúci vyhlasuje, že takéto výslovné zmluvné dojednanie dlhšej lehoty na splnenie peňažného záväzku nie je v hrubom nepomere k jeho právam a povinnostiam vyplývajúcim mu z tohto záväzkového vzťahu (podľa § 369d Obchodného zákonníka), a že takéto osobitné dojednanie odôvodňuje povaha predmetu plnenia záväzku. Kupujúci zaplatí predávajúcemu kúpnu cenu za dodaný tovar bezhotovostne – prevodom na účet predávajúceho. Kupujúci preddavky z kúpnej ceny predávajúcemu neposkytuje. Za deň úhrady faktúry (deň zaplatenia kúpnej ceny za tovar) sa pre účely tejto rámcovej dohody rozumie deň pripísania fakturovanej sumy na účet predávajúceho.
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      <cbc:Description languageID="SLK"><![CDATA[Predmetom zákazky je: Liek s účinnou látkou palivizumab 
Palivizumab je rekombinantná humanizovaná monoklonálna protilátka vyrobená technológiou DNA v hostiteľských bunkách myelómu myší.
Jedna 0,5 ml injekčná liekovka obsahuje 50 mg palivizumabu
Liek je indikovaný na prevenciu závažného ochorenia dolných dýchacích ciest vyžadujúceho hospitalizáciu, ktoré je vyvolané respiračným syncyciálnym vírusom (RSV) u detí s vysokým rizikom ochorenia RSV: 
• deti, ktoré sa narodili v 35. týždni gravidity alebo skôr a na začiatku sezóny RSV sú mladšie ako 6 mesiacov; 
• deti do 2 rokov, u ktorých bola v posledných 6 mesiacoch potrebná liečba bronchopulmonálnej dysplázie; 
• deti do 2 rokov s hemodynamicky signifikantným vrodeným srdcovým ochorením
]]></cbc:Description>
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         <cbc:Description languageID="SLK"><![CDATA[Predmetom zákazky je: Liek s účinnou látkou palivizumab 
Palivizumab je rekombinantná humanizovaná monoklonálna protilátka vyrobená technológiou DNA v hostiteľských bunkách myelómu myší.
Jedna 0,5 ml injekčná liekovka obsahuje 50 mg palivizumabu
Liek je indikovaný na prevenciu závažného ochorenia dolných dýchacích ciest vyžadujúceho hospitalizáciu, ktoré je vyvolané respiračným syncyciálnym vírusom (RSV) u detí s vysokým rizikom ochorenia RSV: 
• deti, ktoré sa narodili v 35. týždni gravidity alebo skôr a na začiatku sezóny RSV sú mladšie ako 6 mesiacov; 
• deti do 2 rokov, u ktorých bola v posledných 6 mesiacoch potrebná liečba bronchopulmonálnej dysplázie; 
• deti do 2 rokov s hemodynamicky signifikantným vrodeným srdcovým ochorením
]]></cbc:Description>
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