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Cel zam\u00f3wienia\nCelem zam\u00f3wienia jest:\n\u2022\tzapewnienie elektronicznej ewidencji ankiet endoprotezoplastyki,\n\u2022\tautomatyzacja raportowania danych do Rejestru Endoprotezoplastyk,\n\u2022\tograniczenie r\u0119cznego wprowadzania danych,\n\u2022\tpoprawa jako\u015bci i kompletno\u015bci danych medycznych,\n\u2022\tzapewnienie zgodno\u015bci z obowi\u0105zuj\u0105cymi standardami bezpiecze\u0144stwa i RODO.\n3. Zakres funkcjonalny systemu\nSystem musi spe\u0142nia\u0107 wymagania funkcjonalne okre\u015blone w Specyfikacji Rejestru Endoprotezoplastyk stanowi\u0105cej za\u0142\u0105cznik do post\u0119powania, w szczeg\u00f3lno\u015bci:\n3.1 Ewidencja danych medycznych\nSystem musi zapewnia\u0107:\n\u2022\tewidencj\u0119 ankiet endoprotezoplastyki,\n\u2022\tobs\u0142ug\u0119 r\u00f3\u017cnych typ\u00f3w ankiet (pe\u0142nych i rozliczeniowych),\n\u2022\tpodpowiadanie danych pacjenta,\n\u2022\tkopiowanie danych medycznych i lek\u00f3w z historii leczenia,\n\u2022\tautoryzacj\u0119 i podpis elektroniczny ankiet.\n3.2 Integracja z Rejestrem Endoprotezoplastyk (RE)\nSystem musi umo\u017cliwia\u0107:\n\u2022\tlogowanie i uwierzytelnianie u\u017cytkownik\u00f3w w systemie RE,\n\u2022\twysy\u0142k\u0119 ankiet do Rejestru Endoprotezoplastyk,\n\u2022\tobs\u0142ug\u0119 komunikacji z systemem RE,\n\u2022\tobs\u0142ug\u0119 b\u0142\u0119d\u00f3w zwracanych przez RE,\n\u2022\twalidacj\u0119 danych przed wysy\u0142k\u0105.\n3.3 Integracja z systemami Zamawiaj\u0105cego\nWykonawca zapewni integracj\u0119 systemu z:\n\u2022\tsystemem HIS funkcjonuj\u0105cym u Zamawiaj\u0105cego,\n\u2022\tbaz\u0105 danych pacjent\u00f3w,\n\u2022\tdokumentacj\u0105 medyczn\u0105.\nIntegracja powinna umo\u017cliwia\u0107 automatyczne pobieranie danych medycznych bez konieczno\u015bci ich ponownego wprowadzania.\n3.4 Wdro\u017cenie systemu\nWdro\u017cenie obejmuje:\n\u2022\tinstalacj\u0119 oprogramowania,\n\u2022\tkonfiguracj\u0119 \u015brodowiska produkcyjnego,\n\u2022\tkonfiguracj\u0119 komunikacji z RE,\n\u2022\ttesty funkcjonalne i integracyjne,\n\u2022\turuchomienie systemu.\nWarunkiem odbioru b\u0119dzie pozytywny wynik test\u00f3w akceptacyjnych.\n3.5 Szkolenia\nWykonawca przeprowadzi szkolenia dla:\n\u2022\tu\u017cytkownik\u00f3w medycznych,\n\u2022\tadministrator\u00f3w systemu.\nSzkolenia musz\u0105 obejmowa\u0107 obs\u0142ug\u0119 ankiet, autoryzacj\u0119 danych oraz procedury wysy\u0142ki do RE.\n3.6 Dokumentacja\nWykonawca dostarczy:\n\u2022\tdokumentacj\u0119 u\u017cytkow\u0105,\n\u2022\tdokumentacj\u0119 techniczn\u0105,\n\u2022\tinstrukcje integracyjne,\n\u2022\tprocedury awaryjne.\n3.7 Wsparcie i gwarancja\nSystem musi by\u0107 obj\u0119ty:\n\u2022\tminimum 36-miesi\u0119czn\u0105 gwarancj\u0105,\n\u2022\twsparciem technicznym,\n\u2022\taktualizacjami systemu wynikaj\u0105cymi ze zmian po stronie Rejestru Endoprotezoplastyk.\n4. Wymagania techniczne i prawne\nSystem musi:\n\u2022\tdzia\u0142a\u0107 w infrastrukturze Zamawiaj\u0105cego,\n\u2022\tby\u0107 zgodny z przepisami RODO,\n\u2022\tzapewnia\u0107 bezpiecze\u0144stwo danych medycznych,\n\u2022\tumo\u017cliwia\u0107 autoryzacj\u0119 u\u017cytkownik\u00f3w i rejestrowanie operacji.\nUwaga!\nJe\u017celi w specyfikacji przedstawionej w za\u0142. 1a pojawiaj\u0105 si\u0119 odniesienia do konkretnych marek, znak\u00f3w towarowych, patent\u00f3w czy pochodzenia produkt\u00f3w, nale\u017cy je traktowa\u0107 wy\u0142\u0105cznie jako przyk\u0142adowe, maj\u0105ce na celu okre\u015blenie oczekiwanych standard\u00f3w jako\u015bciowych. 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