{"id":4305,"date":"2019-05-15T18:31:24","date_gmt":"2019-05-15T15:31:24","guid":{"rendered":"https:\/\/www.norameda.com\/jakosc\/"},"modified":"2019-07-02T13:27:21","modified_gmt":"2019-07-02T10:27:21","slug":"jakosc","status":"publish","type":"page","link":"https:\/\/www.norameda.com\/pl\/jakosc\/","title":{"rendered":"Jako\u015b\u0107"},"content":{"rendered":"

[et_pb_section bb_built=”1″ fullwidth=”on” _builder_version=”3.0.82″ next_background_color=”#000000″ inner_width=”auto” inner_max_width=”1080px”][et_pb_fullwidth_image src=”https:\/\/www.norameda.com\/wp-content\/uploads\/2018\/08\/apie-mus-headeris.png” _builder_version=”3.9″ \/][\/et_pb_section][et_pb_section bb_built=”1″ fullwidth=”off” specialty=”off” _builder_version=”3.0.98″ module_class=”yoastBreadcrumb” prev_background_color=”#000000″ next_background_color=”#000000″ inner_width=”auto” inner_max_width=”1080px”][et_pb_row background_position=”top_left” background_repeat=”repeat” background_size=”initial”][et_pb_column type=”4_4″][et_pb_code _builder_version=”3.0.98″]Strona G\u0142\u00f3wna<\/a><\/span>[\/et_pb_code][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section bb_built=”1″ _builder_version=”3.0.92″ custom_padding=”50px|0px|13px|0px” prev_background_color=”#000000″ next_background_color=”#000000″ inner_width=”auto” inner_max_width=”1080px”][et_pb_row _builder_version=”3.0.82″ width=”80%” max_width=”1080px”][et_pb_column type=”4_4″][et_pb_cta title=”JAKO\u015a\u0106” use_background_color=”off” background_layout=”light” _builder_version=”3.0.92″ text_orientation=”left” url_new_window=”off” custom_button=”off” button_icon_placement=”right” header_font=”Roboto Condensed||||||||” header_font_size=”36″ header_text_color=”#5e5e5e” button_text_size__hover_enabled=”off” button_text_size__hover=”null” button_one_text_size__hover_enabled=”off” button_one_text_size__hover=”null” button_two_text_size__hover_enabled=”off” button_two_text_size__hover=”null” button_text_color__hover_enabled=”off” button_text_color__hover=”null” button_one_text_color__hover_enabled=”off” button_one_text_color__hover=”null” button_two_text_color__hover_enabled=”off” button_two_text_color__hover=”null” button_border_width__hover_enabled=”off” button_border_width__hover=”null” button_one_border_width__hover_enabled=”off” button_one_border_width__hover=”null” button_two_border_width__hover_enabled=”off” button_two_border_width__hover=”null” button_border_color__hover_enabled=”off” button_border_color__hover=”null” button_one_border_color__hover_enabled=”off” button_one_border_color__hover=”null” button_two_border_color__hover_enabled=”off” button_two_border_color__hover=”null” button_border_radius__hover_enabled=”off” button_border_radius__hover=”null” button_one_border_radius__hover_enabled=”off” button_one_border_radius__hover=”null” button_two_border_radius__hover_enabled=”off” button_two_border_radius__hover=”null” button_letter_spacing__hover_enabled=”off” button_letter_spacing__hover=”null” button_one_letter_spacing__hover_enabled=”off” button_one_letter_spacing__hover=”null” button_two_letter_spacing__hover_enabled=”off” button_two_letter_spacing__hover=”null” button_bg_color__hover_enabled=”off” button_bg_color__hover=”null” button_one_bg_color__hover_enabled=”off” button_one_bg_color__hover=”null” button_two_bg_color__hover_enabled=”off” button_two_bg_color__hover=”null” \/][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section bb_built=”1″ _builder_version=”3.9″ custom_padding=”12.625px|0px|40px|0px” prev_background_color=”#000000″ next_background_color=”#000000″ inner_width=”auto” inner_max_width=”1080px”][et_pb_row _builder_version=”3.0.98″ module_class_1=”quality” width=”80%” max_width=”1080px”][et_pb_column type=”4_4″][et_pb_text _builder_version=”3.9″ text_font=”Open Sans||||”]<\/p>\n

W ca\u0142ej Unii Europejskiej przemys\u0142 farmaceutyczny i dystrybucja lek\u00f3w podlega wysokim normom zapewnienia jako\u015bci, dzi\u0119ki czemu osoby kupuj\u0105ce i stosuj\u0105ce leki mog\u0105 by\u0107 pewne ich jako\u015bci, bezpiecze\u0144stwa i skuteczno\u015bci. Wszystkie produkty lecznicze wytwarzane i wprowadzane do obrotu w Unii Europejskiej s\u0105 oceniane przez upowa\u017cnione instytucje i wprowadzane na rynek po spe\u0142nieniu rygorystycznych wymaga\u0144. Gwarancj\u0105 spe\u0142nienia tych wymaga\u0144 s\u0105 okre\u015blone certyfikaty i licencje. Jednym z g\u0142\u00f3wnych cel\u00f3w \u201eNoramedy\u201d jest zapewnienie wysokiej jako\u015bci produkt\u00f3w, kt\u00f3rej gwarancj\u0105 s\u0105 posiadane certyfikaty i licencje.<\/p>\n

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box_shadow_vertical_tablet=”0px” box_shadow_blur_tablet=”40px” box_shadow_spread_tablet=”0px” z_index_tablet=”500″]<\/p>\n

LICENCJA PRODUKCYJNA<\/h3>\n

Wytw\u00f3rcy produkt\u00f3w leczniczych w Unii Europejskiej oraz importerzy tych\u017ce wyrob\u00f3w z kraj\u00f3w trzecich powinni posiada\u0107 licencj\u0119 produkcyjn\u0105. Licencja produkcyjna pozwala na sprzeda\u017c lek\u00f3w w\u0142asnej produkcji lub importowanych zgodnie z Dobrymi Praktykami Dystrybucyjnymi.<\/span><\/p>\n

Licencja produkcyjna \u201eNoramedy\u201d <\/a><\/p>\n

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ZEZWOLENIE NA PROWADZENIE OBROTU HURTOWEGO PRODUKTAMI LECZNICZYMI<\/h3>\n

Zezwolenie na prowadzenie obrotu hurtowego produktami leczniczymi pozwala na sprzeda\u017c hurtow\u0105 w deklarowanym miejscu zgodnie z obowi\u0105zuj\u0105cymi w bran\u017cy farmaceutycznej aktami prawnymi. Zezwolenie zostanie wydane po upewnieniu si\u0119, \u017ce dystrybutor produkt\u00f3w leczniczych posiada odpowiednie pomieszczenie i urz\u0105dzenia, przestrzega wymaga\u0144 dotycz\u0105cych systemu zarz\u0105dzania jako\u015bci\u0105, spe\u0142nia warunki doboru personelu, zarz\u0105dzania dokumentami, wykonywanych transakcji, skarg i za\u017cale\u0144, domniemanych falsyfikat\u00f3w, ma regu\u0142y reklamacji substancji czynnych i ich wycofania, dzia\u0142alno\u015bci umownej, audyt\u00f3w wewn\u0119trznych.<\/span><\/p>\n

Zezwolenie na prowadzenie obrotu hurtowego produktami leczniczymi \u201eNoramedy\u201d a<\/a><\/p>\n

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CERTYFIKAT DOBRYCH PRAKTYK DYSTRYBUCYJNYCH<\/h3>\n

Dobre Praktyki Dystrybucyjne (GDP) oznaczaj\u0105, \u017ce jako\u015b\u0107 lek\u00f3w zostanie zachowana na ka\u017cdym etapie dystrybucji \u2013 od produkcji do miejsca sprzeda\u017cy. Certyfikat Dobrych Praktyk Dystrybucyjnych (certyfikat GDP) \u2013 to dokument wydany przez Krajow\u0105 Agencj\u0119 Kontroli Lek\u00f3w przy Ministerstwie Ochrony Zdrowia Republiki Litewskiej, potwierdzaj\u0105cy, \u017ce dzia\u0142alno\u015b\u0107 farmaceutyczna podmiotu posiadaj\u0105cego certyfikat jest zgodna z wymaganiami dotycz\u0105cymi GDP produkt\u00f3w leczniczych.<\/span><\/p>\n

Certyfikat Dobrych Praktyk Dystrybucyjnych \u201eNoramedy\u201d <\/a><\/p>\n

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CERTYFIKAT DOBREJ PRAKTYKI PRODUKCYJNEJ<\/h3>\n

Dobra Praktyka Produkcyjna (GMP) daje gwarancj\u0119, \u017ce produkcja oraz import produkt\u00f3w leczniczych z kraj\u00f3w trzecich jest zgodny z obowi\u0105zuj\u0105cym standardem jako\u015bci i spe\u0142nia wymagania dotycz\u0105ce przeznaczenia produkt\u00f3w leczniczych, dopuszczenia do obrotu i specyfikacji. Certyfikat Dobrej Praktyki Produkcyjnej (certyfikat GMP) \u2013 to dokument wydany przez Krajow\u0105 Agencj\u0119 Kontroli Lek\u00f3w przy Ministerstwie Ochrony Zdrowia Republiki Litewskiej, potwierdzaj\u0105cy, \u017ce dzia\u0142alno\u015b\u0107 farmaceutyczna lub cz\u0119\u015b\u0107 dzia\u0142alno\u015bci podmiotu posiadaj\u0105cego certyfikat jest zgodna z wymaganiami dotycz\u0105cymi GMP.<\/span><\/p>\n

Certyfikat Dobrej Praktyki Produkcyjnej \u201eNoramedy\u201d
\n<\/a><\/p>\n

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\u015aWIADECTWO PODMIOTU UPRAWNIONEGO DO PRZETWARZANIA \u017bYWNO\u015aCI<\/h3>\n

\u015awiadectwo podmiotu uprawnionego do przetwarzania \u017cywno\u015bci \u2013 to dokument wydany przez Pa\u0144stwow\u0105 S\u0142u\u017cb\u0119 Sanitarno-Epidemiologiczn\u0105, potwierdzaj\u0105ce uprawnienia podmiotu do wykonywania dzia\u0142alno\u015bci, w tym do przetwarzania \u017cywno\u015bci oraz dystrybucji. Dokument zostanie wydany w przypadku spe\u0142nienia obowi\u0105zuj\u0105cych norm sanitarnych oraz wymog\u00f3w zawartych w aktach prawnych.<\/span><\/p>\n

\u015awiadectwo podmiotu uprawnionego do przetwarzania \u017cywno\u015bci \u201eNoramedy\u201d <\/a><\/p>\n

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