{"id":18476,"date":"2024-09-20T12:05:50","date_gmt":"2024-09-20T10:05:50","guid":{"rendered":"https:\/\/episkeymedical.com\/casa\/"},"modified":"2025-03-20T17:23:59","modified_gmt":"2025-03-20T16:23:59","slug":"casa","status":"publish","type":"page","link":"https:\/\/episkeymedical.com\/pt-pt\/","title":{"rendered":"Casa"},"content":{"rendered":"

[et_pb_section fb_built=”1″ _builder_version=”4.26.0″ background_color=”#FFFFFF” background_enable_image=”off” parallax=”on” global_colors_info=”{}”][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.26.0″ _module_preset=”default” custom_margin=”-50px||-20px||false|false” custom_padding=”0px||||false|false” animation_style=”slide” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” text_font=”Arial|700|||||||” header_font=”Arial|800|||||||” header_text_color=”#009ee3″ header_font_size=”48px” custom_margin=”50px||||false|false” global_colors_info=”{}”]<\/p>\n

<\/span>Consultoria em dispositivos m\u00e9dicos<\/span><\/strong><\/h1>\n

[\/et_pb_text][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” text_text_color=”#009ee3″ text_font_size=”20px” global_colors_info=”{}”]<\/p>\n

A melhor forma de garantir que os dispositivos m\u00e9dicos cumprem os requisitos regulamentares internacionais \u00e9 atrav\u00e9s de um servi\u00e7o de consultoria em dispositivos m\u00e9dicos.<\/span><\/p>\n

[\/et_pb_text][et_pb_button button_text=”L\u00ea mais” _builder_version=”4.26.0″ _module_preset=”default” custom_button=”on” button_text_color=”#009ee3″ button_border_radius=”4px” button_letter_spacing=”1px” button_font=”Arial|600|||||||” global_colors_info=”{}”][\/et_pb_button][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_image src=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2025\/02\/EpisKey-Logotipo-animado_500px.gif” title_text=”EpisKey – Logotipo animado_500px” _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ _builder_version=”4.26.0″ _module_preset=”default” background_image=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/07\/GettyImages-1059960534.jpg” parallax=”on” min_height=”760px” global_colors_info=”{}”][et_pb_row _builder_version=”4.26.0″ _module_preset=”default” locked=”off” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” text_text_color=”#009ee3″ header_2_font=”Arial|600|||||||” header_2_text_color=”#009ee3″ header_2_font_size=”50px” global_colors_info=”{}”]<\/p>\n

<\/span><\/span><\/span>Os nossos servi\u00e7os<\/span><\/h2>\n

[\/et_pb_text][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” text_text_color=”#2b435e” global_colors_info=”{}”]<\/p>\n

<\/span><\/span>Oferecemos os melhores servi\u00e7os de consultoria em dispositivos m\u00e9dicos.<\/span><\/p>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_3,1_3,1_3″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”1_3″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_image src=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/07\/Icono-1-blue2.png” title_text=”\u00cdcone 1-azul2″ align=”center” _builder_version=”4.26.0″ _module_preset=”default” background_color=”rgba(255,255,255,0.5)” custom_padding=”20px|20px||20px|false|false” border_radii=”off|4px|4px||” global_colors_info=”{}”][\/et_pb_image][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” background_color=”rgba(255,255,255,0.5)” custom_margin=”-30px||||false|false” custom_padding=”20px|20px||20px|false|false” global_colors_info=”{}”]<\/p>\n

<\/span><\/span>Marca\u00e7\u00e3o CE
para dispositivos m\u00e9dicos<\/strong><\/span><\/h2>\n

[\/et_pb_text][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” background_color=”rgba(255,255,255,0.5)” custom_margin=”-30px||||false|false” custom_padding=”10px|20px|20px|20px|false|false” border_radii=”off|||4px|4px” global_colors_info=”{}”]<\/p>\n

Os nossos especialistas explicam-te como elaborar planos de desenvolvimento, de usabilidade e de valida\u00e7\u00e3o de software.<\/span><\/p>\n

[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_3″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_image src=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/07\/Icono-2-blue2.png” title_text=”\u00cdcone 2-azul2″ align=”center” _builder_version=”4.26.0″ _module_preset=”default” background_color=”rgba(255,255,255,0.5)” custom_padding=”20px|20px||20px|false|false” border_radii=”off|4px|4px||” global_colors_info=”{}”][\/et_pb_image][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” background_color=”rgba(255,255,255,0.5)” custom_margin=”-30px||||false|false” custom_padding=”20px|20px||20px|false|false” global_colors_info=”{}”]<\/p>\n

<\/span>Estrat\u00e9gia
<\/strong><\/span>estrat\u00e9gia<\/strong><\/span><\/h2>\n

[\/et_pb_text][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” background_color=”rgba(255,255,255,0.5)” custom_margin=”-30px||||false|false” custom_padding=”10px|20px|20px|20px|false|false” border_radii=”off|||4px|4px” global_colors_info=”{}”]<\/p>\n

Comercializa\u00e7\u00e3o noutros mercados. Registo de produtos. Estrat\u00e9gias de entrada em pa\u00edses terceiros. <\/span><\/p>\n

[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_3″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_image src=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/07\/Icono-3-blue2.png” title_text=”\u00cdcone 3-azul2″ align=”center” _builder_version=”4.26.0″ _module_preset=”default” background_color=”rgba(255,255,255,0.5)” custom_padding=”20px|20px||20px|false|false” border_radii=”off|4px|4px||” global_colors_info=”{}”][\/et_pb_image][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” background_color=”rgba(255,255,255,0.5)” custom_margin=”-30px||||false|false” custom_padding=”20px|20px||20px|false|false” global_colors_info=”{}”]<\/p>\n

<\/span>Sistemas de Gest\u00e3o da Qualidade ISO 13485
<\/strong><\/span><\/h2>\n

[\/et_pb_text][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” background_color=”rgba(255,255,255,0.5)” custom_margin=”-30px||||false|false” custom_padding=”10px|20px|20px|20px|false|false” border_radii=”off|||4px|4px” global_colors_info=”{}”]<\/p>\n

Plano de avalia\u00e7\u00e3o cl\u00ednica e avalia\u00e7\u00e3o de desempenho Procuramos a melhor estrat\u00e9gia cl\u00ednica.<\/span><\/p>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_button button_url=”\/pt-pt\/servicos\/” button_text=”Ver mais servi\u00e7os” button_alignment=”center” _builder_version=”4.26.0″ _module_preset=”default” custom_button=”on” button_text_color=”#009ee3″ button_border_radius=”4px” button_letter_spacing=”1px” button_font=”Arial|600|||||||” locked=”off” global_colors_info=”{}”][\/et_pb_button][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”3_5,2_5″ disabled_on=”on|on|off” _builder_version=”4.26.0″ _module_preset=”default” custom_margin=”40px||||false|false” custom_padding=”0px||0px||false|false” global_colors_info=”{}”][et_pb_column type=”3_5″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

<\/span>Estrat\u00e9gias de regulamenta\u00e7\u00e3o<\/strong><\/span><\/h2>\n

<\/strong><\/span><\/p>\n

Por fim, a consultoria em dispositivos m\u00e9dicos tamb\u00e9m engloba o desenvolvimento de estrat\u00e9gias regulamentares. Isto inclui assist\u00eancia na identifica\u00e7\u00e3o da classe de risco do produto e na conce\u00e7\u00e3o da estrat\u00e9gia mais adequada para obter as provas cl\u00ednicas necess\u00e1rias para obter a marca\u00e7\u00e3o CE. Em primeiro lugar, \u00e9 necess\u00e1rio garantir que o produto fabricado \u00e9 efetivamente um dispositivo m\u00e9dico. Segue-se a classifica\u00e7\u00e3o de acordo com o n\u00edvel de risco. <\/span><\/p>\n

Para reunir provas cl\u00ednicas, podem ser seguidos diferentes caminhos, incluindo a investiga\u00e7\u00e3o cl\u00ednica, o planeamento de estrat\u00e9gias de entrada e o desenvolvimento de materiais de marketing que cumpram os regulamentos relativos \u00e0 publicidade. Os consultores podem oferecer aconselhamento sobre como posicionar um produto num mercado competitivo, como gerir a propriedade intelectual e como cumprir os regulamentos relacionados com a publicidade e a promo\u00e7\u00e3o. <\/span><\/p>\n

[\/et_pb_text][\/et_pb_column][et_pb_column type=”2_5″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_image src=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/12\/back-img-over-2.png” title_text=”GettyImages-1798796898″ _builder_version=”4.26.0″ _module_preset=”default” background_image=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/09\/GettyImages-1798796898.jpg” min_height=”400px” border_radii=”on|4px|4px|4px|4px” global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”2_5,3_5″ disabled_on=”off|off|on” _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”2_5″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_image src=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/12\/back-img-over-2.png” title_text=”GettyImages-1798796898″ _builder_version=”4.26.0″ _module_preset=”default” background_image=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/09\/GettyImages-1798796898.jpg” max_height=”200px” border_radii=”on|4px|4px|4px|4px” global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][et_pb_column type=”3_5″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

Estrat\u00e9gias de regulamenta\u00e7\u00e3o<\/strong><\/span><\/h2>\n

<\/strong><\/span><\/p>\n

Por fim, a consultoria em dispositivos m\u00e9dicos tamb\u00e9m engloba o desenvolvimento de estrat\u00e9gias regulamentares. Isto inclui assist\u00eancia na identifica\u00e7\u00e3o da classe de risco do produto e na conce\u00e7\u00e3o da estrat\u00e9gia mais adequada para obter as provas cl\u00ednicas necess\u00e1rias para obter a marca\u00e7\u00e3o CE. Em primeiro lugar, \u00e9 necess\u00e1rio garantir que o produto fabricado \u00e9 efetivamente um dispositivo m\u00e9dico. De seguida, procede-se \u00e0 classifica\u00e7\u00e3o de acordo com o n\u00edvel de risco. <\/span><\/p>\n

Para reunir provas cl\u00ednicas, podem ser seguidos diferentes caminhos, incluindo a investiga\u00e7\u00e3o cl\u00ednica, o planeamento de estrat\u00e9gias de entrada e o desenvolvimento de materiais de marketing que cumpram os regulamentos relativos \u00e0 publicidade. Os consultores podem oferecer conselhos sobre como posicionar um produto num mercado competitivo, como gerir a propriedade intelectual e como cumprir os regulamentos relacionados com a publicidade e a promo\u00e7\u00e3o. <\/span><\/p>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”2_5,3_5″ disabled_on=”on|on|off” _builder_version=”4.26.0″ _module_preset=”default” custom_margin=”40px||||false|false” global_colors_info=”{}”][et_pb_column type=”2_5″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_image src=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/12\/back-img-over-2.png” title_text=”GettyImages-867128702″ _builder_version=”4.26.0″ _module_preset=”default” background_image=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/09\/GettyImages-867128702.jpg” min_height=”380px” border_radii=”on|4px|4px|4px|4px” global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][et_pb_column type=”3_5″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

Gest\u00e3o de riscos <\/strong><\/span>gest\u00e3o de riscos<\/strong><\/span><\/span><\/h2>\n

<\/strong><\/span><\/span><\/p>\n

A gest\u00e3o dos riscos \u00e9 uma componente essencial da consultoria em mat\u00e9ria de dispositivos m\u00e9dicos. Os dispositivos m\u00e9dicos devem ser seguros para os pacientes e utilizadores, o que implica identificar, avaliar e atenuar os riscos associados \u00e0 sua utiliza\u00e7\u00e3o. Todo este processo deve ser efectuado de acordo com os princ\u00edpios da norma ISO 14971. <\/span><\/p>\n

Os nossos consultores ajudam as empresas a desenvolver planos de gest\u00e3o do risco, que incluem a identifica\u00e7\u00e3o dos perigos, a an\u00e1lise da probabilidade e da gravidade, a implementa\u00e7\u00e3o de controlos para minimizar o risco e a an\u00e1lise do risco residual. Este processo \u00e9 fundamental n\u00e3o s\u00f3 para a conformidade regulamentar, mas tamb\u00e9m para garantir a confian\u00e7a dos consumidores e a reputa\u00e7\u00e3o da empresa. <\/span><\/p>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”2_5,3_5″ disabled_on=”off|off|on” _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”2_5″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_image src=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/12\/back-img-over-2.png” title_text=”GettyImages-867128702″ _builder_version=”4.26.0″ _module_preset=”default” background_image=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/09\/GettyImages-867128702.jpg” max_height=”200px” border_radii=”on|4px|4px|4px|4px” global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][et_pb_column type=”3_5″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

Gest\u00e3o de riscos <\/strong><\/span>gest\u00e3o de riscos<\/strong><\/span><\/span><\/h2>\n

<\/strong><\/span><\/span><\/p>\n

A gest\u00e3o dos riscos \u00e9 uma componente essencial da consultoria em mat\u00e9ria de dispositivos m\u00e9dicos. Os dispositivos m\u00e9dicos devem ser seguros para os pacientes e utilizadores, o que implica identificar, avaliar e atenuar os riscos associados \u00e0 sua utiliza\u00e7\u00e3o. Todo este processo deve ser efectuado de acordo com os princ\u00edpios da norma ISO 14971. <\/span><\/p>\n

Os nossos consultores ajudam as empresas a desenvolver planos de gest\u00e3o do risco, que incluem a identifica\u00e7\u00e3o dos perigos, a an\u00e1lise da probabilidade e da gravidade, a implementa\u00e7\u00e3o de controlos para minimizar o risco e a an\u00e1lise do risco residual. Este processo \u00e9 fundamental n\u00e3o s\u00f3 para a conformidade regulamentar, mas tamb\u00e9m para garantir a confian\u00e7a dos consumidores e a reputa\u00e7\u00e3o da empresa. <\/span><\/p>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”3_5,2_5″ disabled_on=”on|on|off” _builder_version=”4.26.0″ _module_preset=”default” custom_margin=”40px||||false|false” global_colors_info=”{}”][et_pb_column type=”3_5″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

Documenta\u00e7\u00e3o <\/span><\/strong>t\u00e9cnica<\/span><\/strong><\/span><\/h2>\n

<\/span><\/strong><\/span><\/p>\n

Se um fabricante de dispositivos m\u00e9dicos quiser resolver com \u00eaxito a avalia\u00e7\u00e3o do seu produto para certificar a conformidade com o regulamento, \u00e9 necess\u00e1rio apresentar de forma ordenada todas as provas documentais que garantam a conformidade com os requisitos. Por conseguinte, a prepara\u00e7\u00e3o e manuten\u00e7\u00e3o da documenta\u00e7\u00e3o t\u00e9cnica \u00e9 um requisito indispens\u00e1vel para a conformidade regulamentar. <\/span><\/p>\n

Esta documenta\u00e7\u00e3o inclui uma descri\u00e7\u00e3o detalhada do produto, dados de conce\u00e7\u00e3o, resultados de investiga\u00e7\u00e3o cl\u00ednica e testes de conformidade, entre outros. A consultoria em dispositivos m\u00e9dicos fornece suporte na prepara\u00e7\u00e3o dessa documenta\u00e7\u00e3o, garantindo que ela seja completa, precisa e esteja em conformidade com os requisitos regulamentares. Isto \u00e9 crucial para o processo de avalia\u00e7\u00e3o da conformidade e para a obten\u00e7\u00e3o das marca\u00e7\u00f5es CE ou das aprova\u00e7\u00f5es da FDA. <\/span><\/p>\n

[\/et_pb_text][\/et_pb_column][et_pb_column type=”2_5″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_image src=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/12\/back-img-over-2.png” title_text=”GettyImages-649235634″ _builder_version=”4.26.0″ _module_preset=”default” background_image=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/09\/GettyImages-649235634.jpg” min_height=”390px” border_radii=”on|4px|4px|4px|4px” global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”2_5,3_5″ disabled_on=”off|off|on” _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”2_5″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_image src=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/12\/back-img-over-2.png” title_text=”GettyImages-649235634″ _builder_version=”4.26.0″ _module_preset=”default” background_image=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/09\/GettyImages-649235634.jpg” max_height=”200px” border_radii=”on|4px|4px|4px|4px” global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][et_pb_column type=”3_5″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

Documenta\u00e7\u00e3o <\/span><\/strong>t\u00e9cnica<\/span><\/strong><\/span><\/h2>\n

<\/span><\/strong><\/span><\/p>\n

Se um fabricante de dispositivos m\u00e9dicos quiser resolver com \u00eaxito a avalia\u00e7\u00e3o do seu produto para certificar a conformidade com o regulamento, \u00e9 necess\u00e1rio apresentar de forma ordenada todas as provas documentais que garantam a conformidade com os requisitos. Por conseguinte, a prepara\u00e7\u00e3o e manuten\u00e7\u00e3o da documenta\u00e7\u00e3o t\u00e9cnica \u00e9 um requisito indispens\u00e1vel para a conformidade regulamentar. <\/span><\/p>\n

Esta documenta\u00e7\u00e3o inclui uma descri\u00e7\u00e3o detalhada do produto, dados de conce\u00e7\u00e3o, resultados de investiga\u00e7\u00e3o cl\u00ednica e testes de conformidade, entre outros. A consultoria em dispositivos m\u00e9dicos fornece suporte na prepara\u00e7\u00e3o dessa documenta\u00e7\u00e3o, garantindo que ela seja completa, precisa e esteja em conformidade com os requisitos regulamentares. Isto \u00e9 crucial para o processo de avalia\u00e7\u00e3o da conformidade e para a obten\u00e7\u00e3o das marca\u00e7\u00f5es CE ou das aprova\u00e7\u00f5es da FDA. <\/span><\/p>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”2_5,3_5″ disabled_on=”on|on|off” _builder_version=”4.26.0″ _module_preset=”default” custom_margin=”40px||||false|false” global_colors_info=”{}”][et_pb_column type=”2_5″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_image src=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/12\/back-img-over-2.png” title_text=”GettyImages-909908830″ _builder_version=”4.26.0″ _module_preset=”default” background_image=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/09\/GettyImages-909908830.jpg” min_height=”407px” border_radii=”on|4px|4px|4px|4px” global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][et_pb_column type=”3_5″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

Investiga\u00e7\u00e3o <\/span><\/strong>cl\u00ednicas<\/span><\/strong><\/span><\/strong><\/span><\/h2>\n

<\/span><\/strong><\/span><\/p>\n

Nalguns casos, quando o grau de risco para o doente o exige, s\u00e3o necess\u00e1rias investiga\u00e7\u00f5es cl\u00ednicas para demonstrar o benef\u00edcio cl\u00ednico do produto. Noutros casos, os fabricantes pretendem confirmar a utiliza\u00e7\u00e3o prevista atrav\u00e9s da investiga\u00e7\u00e3o. Em resumo, as investiga\u00e7\u00f5es cl\u00ednicas s\u00e3o essenciais para demonstrar a seguran\u00e7a e a efic\u00e1cia dos dispositivos m\u00e9dicos, especialmente no caso dos dispositivos de maior risco. <\/span><\/p>\n

Em muitos casos, a investiga\u00e7\u00e3o deve ser autorizada pela Ag\u00eancia Espanhola de Medicamentos e Produtos de Sa\u00fade (AEMPS). Os consultores especializados neste dom\u00ednio podem ajudar as empresas a conceber e a preparar o pedido de autoriza\u00e7\u00e3o da AEMPS. Al\u00e9m disso, podem ajudar na elabora\u00e7\u00e3o dos relat\u00f3rios cl\u00ednicos necess\u00e1rios para os pedidos de autoriza\u00e7\u00e3o. <\/span><\/p>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”2_5,3_5″ disabled_on=”off|off|on” _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”2_5″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_image src=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/12\/back-img-over-2.png” title_text=”GettyImages-909908830″ _builder_version=”4.26.0″ _module_preset=”default” background_image=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/09\/GettyImages-909908830.jpg” max_height=”200px” border_radii=”on|4px|4px|4px|4px” global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][et_pb_column type=”3_5″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

Investiga\u00e7\u00e3o <\/span><\/strong>cl\u00ednicas<\/span><\/strong><\/span><\/strong><\/span><\/h2>\n

 <\/p>\n

Nalguns casos, quando o grau de risco para o doente o exige, s\u00e3o necess\u00e1rias investiga\u00e7\u00f5es cl\u00ednicas para demonstrar o benef\u00edcio cl\u00ednico do produto. Noutros casos, os fabricantes pretendem confirmar a utiliza\u00e7\u00e3o prevista atrav\u00e9s da investiga\u00e7\u00e3o. Em resumo, as investiga\u00e7\u00f5es cl\u00ednicas s\u00e3o essenciais para demonstrar a seguran\u00e7a e a efic\u00e1cia dos dispositivos m\u00e9dicos, especialmente no caso dos dispositivos de maior risco. <\/span><\/p>\n

Em muitos casos, a investiga\u00e7\u00e3o deve ser autorizada pela Ag\u00eancia Espanhola de Medicamentos e Produtos de Sa\u00fade (AEMPS). Os consultores especializados neste dom\u00ednio podem ajudar as empresas a conceber e a preparar o pedido de autoriza\u00e7\u00e3o da AEMPS. Al\u00e9m disso, podem ajudar na elabora\u00e7\u00e3o dos relat\u00f3rios cl\u00ednicos necess\u00e1rios para os pedidos de autoriza\u00e7\u00e3o. <\/span><\/p>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_button button_text=”Gostaria de receber uma proposta” button_alignment=”center” _builder_version=”4.26.0″ _module_preset=”default” custom_button=”on” button_text_color=”#009ee3″ button_border_radius=”4px” button_letter_spacing=”1px” button_font=”Arial|600|||||||” locked=”off” global_colors_info=”{}”][\/et_pb_button][et_pb_divider color=”#2b435e” divider_weight=”2px” _builder_version=”4.26.0″ _module_preset=”default” custom_margin=”60px||||false|false” global_colors_info=”{}”][\/et_pb_divider][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”2_5,3_5″ _builder_version=”4.26.0″ _module_preset=”default” background_color=”rgba(255,255,255,0.4)” border_radii=”on|4px|4px|4px|4px” global_colors_info=”{}”][et_pb_column type=”2_5″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][lwp_overlay_image src=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/07\/Isabel-Lopez-consultora.jpg” overlay_color=”rgba(0,158,227,0.81)” _builder_version=”4.26.0″ _module_preset=”default” module_font=”Arial||||||||” module_text_color=”#FFFFFF” text_orientation=”left” custom_margin=”20px|||40px|false|false” border_radii=”on|4px|4px|4px|4px” global_colors_info=”{}”]<\/p>\n

Isabel L\u00f3pez Guerrero, fundadora e CEO da EpisKey Medical Consulting SL, tem mais de 15 anos de experi\u00eancia no sector farmac\u00eautico e m\u00e9dico, tendo iniciado a sua carreira profissional na T\u00dcV SUD – ATISAE como consultora e auditora em sistemas de qualidade, dispositivos m\u00e9dicos e produtos farmac\u00eauticos.<\/p>\n

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Por detr\u00e1s <\/span>por detr\u00e1s do sucesso<\/span><\/strong><\/span><\/h2>\n

<\/span><\/strong><\/span><\/p>\n

<\/span><\/span>Na EpisKey Medical Consulting trabalhamos com uma equipa de especialistas com uma vasta experi\u00eancia em dispositivos m\u00e9dicos e com uma grande vontade de colaborar. Realizamos projectos para obter a licen\u00e7a de distribui\u00e7\u00e3o de dispositivos m\u00e9dicos, solicitar a marca\u00e7\u00e3o CE necess\u00e1ria para que um dispositivo m\u00e9dico possa ser comercializado na Uni\u00e3o Europeia ou formar os nossos clientes para actuarem como Respons\u00e1veis T\u00e9cnicos do seu produto. <\/span><\/p>\n

Sabemos exatamente como classificar os seus dispositivos m\u00e9dicos de acordo com os novos regulamentos e estamos habituados a trabalhar num ambiente tecnol\u00f3gico e em mudan\u00e7a. Oferecemos solu\u00e7\u00f5es para a ind\u00fastria de dispositivos m\u00e9dicos adaptadas \u00e0 sua situa\u00e7\u00e3o: licen\u00e7as, autoriza\u00e7\u00f5es, regulamentos, certifica\u00e7\u00f5es, etc. <\/span><\/p>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row _builder_version=”4.26.0″ _module_preset=”default” custom_margin=”40px||||false|false” border_radii=”on|4px|4px|4px|4px” border_width_all=”2px” border_color_all=”#009ee3″ locked=”off” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_icon font_icon=”||divi||400″ icon_color=”#009ee3″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][\/et_pb_icon][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” header_2_font=”Arial|600|||||||” header_2_text_color=”#009ee3″ header_2_font_size=”50px” text_orientation=”center” custom_margin=”20px||||false|false” custom_padding=”|40px||40px|false|false” global_colors_info=”{}”]<\/p>\n

<\/span>O que \u00e9 a consultoria<\/span><\/h2>\n

de dispositivos m\u00e9dicos?<\/span><\/h2>\n

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A \u00e1rea da consultoria em dispositivos m\u00e9dicos engloba uma gama de servi\u00e7os especializados prestados a empresas envolvidas no desenvolvimento, fabrico ou distribui\u00e7\u00e3o de dispositivos m\u00e9dicos. Estes servi\u00e7os incluem orienta\u00e7\u00f5es regulamentares, gest\u00e3o de riscos, documenta\u00e7\u00e3o t\u00e9cnica, investiga\u00e7\u00f5es cl\u00ednicas e estrat\u00e9gias para abordar a conformidade regulamentar, entre outros. Os nossos consultores desempenham um papel vital como intermedi\u00e1rios entre as empresas e as autoridades reguladoras, assegurando que os produtos cumprem todos os requisitos legais antes de serem colocados no mercado. <\/span><\/p>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” header_2_font=”Arial|600|||||||” header_2_text_color=”#009ee3″ header_2_font_size=”50px” text_orientation=”center” custom_margin=”20px||||false|false” custom_padding=”|40px||40px|false|false” global_colors_info=”{}”]<\/p>\n

<\/span>Normas e regulamenta\u00e7\u00e3o<\/h2>\n

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Um dos aspectos mais importantes da consultoria em dispositivos m\u00e9dicos \u00e9 a conformidade regulamentar. Na Europa, os dispositivos m\u00e9dicos t\u00eam de cumprir o Regulamento relativo aos dispositivos m\u00e9dicos (MDR 2017\/745) ou o Regulamento relativo ao diagn\u00f3stico in vitro (IVDR 2017\/746), consoante a sua natureza. Estes regulamentos estabelecem requisitos rigorosos para a avalia\u00e7\u00e3o da conformidade, documenta\u00e7\u00e3o t\u00e9cnica e vigil\u00e2ncia p\u00f3s-comercializa\u00e7\u00e3o. Os nossos consultores ajudam as empresas a interpretar e aplicar estes regulamentos, garantindo que os seus produtos podem ser colocados no mercado sem problemas. <\/span><\/p>\n

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Noutros mercados, como o dos Estados Unidos, a Food and Drug Administration (FDA) \u00e9 a principal autoridade reguladora. A consultoria neste contexto envolve a orienta\u00e7\u00e3o das empresas atrav\u00e9s do processo de autoriza\u00e7\u00e3o 510(k) ou de pedido de aprova\u00e7\u00e3o antes da comercializa\u00e7\u00e3o (PMA), assegurando que os produtos cumprem as normas de seguran\u00e7a e efic\u00e1cia exigidas. <\/span><\/span><\/p>\n

Tamb\u00e9m ajudamos os nossos clientes a desenvolver sistemas de gest\u00e3o da qualidade que estejam em conformidade com o CRF 21.820.<\/span><\/p>\n

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A consultoria em dispositivos m\u00e9dicos \u00e9 uma ferramenta essencial para as empresas que procuram garantir o sucesso dos seus produtos num ambiente altamente regulamentado. <\/span><\/p>\n

Desde a conformidade regulamentar \u00e0 gest\u00e3o de riscos, documenta\u00e7\u00e3o t\u00e9cnica, ensaios cl\u00ednicos e estrat\u00e9gias de mercado, os nossos consultores oferecem uma abordagem abrangente que ajuda as empresas de dispositivos m\u00e9dicos a ultrapassar desafios e a maximizar o potencial dos seus produtos no mercado global.<\/span><\/p>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ _builder_version=”4.26.0″ _module_preset=”default” background_image=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/07\/GettyImages-1387313636-Convertido.jpg” parallax=”on” global_colors_info=”{}”][et_pb_row _builder_version=”4.26.0″ _module_preset=”default” locked=”off” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” text_text_color=”#2b435e” header_2_font=”Arial|600|||||||” header_2_text_color=”#2b435e” header_2_font_size=”50px” global_colors_info=”{}”]<\/p>\n

<\/span><\/span><\/span>Agradecimentos<\/span><\/h2>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][ba_info_box photo=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/07\/isabel-entrevista-1-1-2048×1334-1.webp” title=”Pr\u00e9mio Internacional de Consultoria Episkey Medical Consulting” body_content=”<\/p>\n

Os Pr\u00e9mios Emprendedoras 2022 tiveram lugar em Madrid, a 6 de outubro. O pr\u00e9mio <\/span>consultoria internacional <\/span>desenvolvido pela Episkey Medical Consulting<\/a> ganhou o segundo pr\u00e9mio para o projeto com maior proje\u00e7\u00e3o internacional gra\u00e7as \u00e0…<\/span><\/p>\n

” content_alignment=”center” btn_spacing_top=”40px” title_bottom_spacing=”20px” _builder_version=”4.26.0″ _module_preset=”default” title_level=”h3″ title_font=”–et_global_heading_font|600|||||||” title_text_align=”left” title_text_color=”#009ee3″ body_text_color=”#2b435e” custom_button=”on” button_text_size=”1rem” button_text_color=”#0770ec” button_bg_color=”#ffffff” button_border_color=”#3979ff” button_border_radius=”2px” button_letter_spacing=”1px” button_font=”–et_global_heading_font|700|||||||” button_use_icon=”off” button_custom_padding=”0.7rem|2rem|0.7rem|2rem|true|true” border_radii_photo=”on|4px|4px|4px|4px” global_colors_info=”{}”][\/ba_info_box][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][ba_info_box photo=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/07\/Foro-innovacion1.jpg” title=”Particip\u00e1mos no f\u00f3rum sobre inova\u00e7\u00e3o e transforma\u00e7\u00e3o digital nos cuidados de sa\u00fade” body_content=”<\/p>\n

As restri\u00e7\u00f5es adoptadas devido \u00e0 pandemia do coronav\u00edrus est\u00e3o a ser gradualmente flexibilizadas. As possibilidades de participar em reuni\u00f5es presenciais est\u00e3o a aumentar. Atrav\u00e9s de <\/span>Ticbiomed<\/a> fomos informados do convite \u00e0 apresenta\u00e7\u00e3o de propostas<\/span>…<\/span><\/p>\n

” content_alignment=”center” btn_spacing_top=”40px” title_bottom_spacing=”20px” _builder_version=”4.26.0″ _module_preset=”default” title_level=”h3″ title_font=”–et_global_heading_font|600|||||||” title_text_align=”left” title_text_color=”#009ee3″ body_text_color=”#2b435e” custom_button=”on” button_text_size=”1rem” button_text_color=”#0770ec” button_bg_color=”#ffffff” button_border_color=”#3979ff” button_border_radius=”2px” button_letter_spacing=”1px” button_font=”–et_global_heading_font|700|||||||” button_use_icon=”off” button_custom_padding=”0.7rem|2rem|0.7rem|2rem|true|true” border_radii_photo=”on|4px|4px|4px|4px” global_colors_info=”{}”][\/ba_info_box][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ _builder_version=”4.26.0″ _module_preset=”default” background_color=”#fffcf9″ background_image=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/08\/testimonios-epis.jpg” global_colors_info=”{}”][et_pb_row _builder_version=”4.26.0″ _module_preset=”default” locked=”off” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” text_text_color=”#2b435e” header_2_font=”Arial|600|||||||” header_2_text_color=”#FFFFFF” header_2_font_size=”50px” global_colors_info=”{}”]<\/p>\n

<\/span>Testemunhos<\/span><\/h2>\n

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Ter um consultor a ajudar-nos com a marca\u00e7\u00e3o CE poupou-nos tempo e deu-nos uma melhor compreens\u00e3o do processo.<\/em><\/p>\n

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A Isabel disse-nos que \u00edamos andar de m\u00e3os dadas e assim foi, estiveram sempre dispon\u00edveis e responderam sempre \u00e0s nossas perguntas.<\/em><\/p>\n

[\/et_pb_testimonial][\/et_pb_column][et_pb_column type=”1_3″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_testimonial quote_icon=”off” quote_icon_color=”RGBA(255,255,255,0)” _builder_version=”4.26.0″ _module_preset=”default” background_color=”rgba(255,255,255,0.5)” border_radii=”on|4px|4px|4px|4px” box_shadow_style=”preset1″ box_shadow_color=”rgba(211,211,211,0.3)” global_colors_info=”{}”]<\/p>\n

A regulamenta\u00e7\u00e3o \u00e9 sempre um mal necess\u00e1rio e, depois de nos termos deparado com ela v\u00e1rias vezes, a Episkey ajudou-nos a compreender o que precis\u00e1vamos e a avan\u00e7ar rapidamente.<\/em><\/p>\n

[\/et_pb_testimonial][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ _builder_version=”4.26.0″ _module_preset=”default” background_image=”https:\/\/episkeymedical.com\/wp-content\/uploads\/2024\/07\/back-6-epi.png” parallax=”on” global_colors_info=”{}”][et_pb_row column_structure=”1_3,1_3,1_3″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”1_3″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_number_counter title=”projectos” number=”132″ percent_sign=”off” _builder_version=”4.26.0″ _module_preset=”default” title_font=”|600|||||||” title_text_color=”#FFFFFF” title_font_size=”24px” number_font=”Work Sans|700|||||||” number_text_color=”#FFFFFF” global_colors_info=”{}”][\/et_pb_number_counter][\/et_pb_column][et_pb_column type=”1_3″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_number_counter title=”sucesso” number=”95″ _builder_version=”4.26.0″ _module_preset=”default” title_font=”|600|||||||” title_text_color=”#FFFFFF” title_font_size=”24px” number_font=”Work Sans|700|||||||” number_text_color=”#FFFFFF” global_colors_info=”{}”][\/et_pb_number_counter][\/et_pb_column][et_pb_column type=”1_3″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_number_counter title=”Marca\u00e7\u00e3o CE” number=”+50″ percent_sign=”off” _builder_version=”4.26.0″ _module_preset=”default” title_font=”|600|||||||” title_text_color=”#FFFFFF” title_font_size=”24px” number_font=”Work Sans|700|||||||” number_text_color=”#FFFFFF” global_colors_info=”{}”][\/et_pb_number_counter][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ _builder_version=”4.26.0″ _module_preset=”default” background_color=”#fffcf9″ global_colors_info=”{}”][et_pb_row _builder_version=”4.26.0″ _module_preset=”default” locked=”off” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” text_text_color=”#2b435e” header_2_font=”Arial|600|||||||” header_2_text_color=”#2b435e” header_2_font_size=”50px” global_colors_info=”{}”]<\/p>\n

<\/span><\/span><\/span>Contacta-nos<\/span><\/h2>\n

[\/et_pb_text][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” text_text_color=”#2b435e” global_colors_info=”{}”]<\/p>\n

<\/span><\/span><\/span>Se tiveres alguma d\u00favida ou quest\u00e3o, contacta-nos preenchendo o seguinte formul\u00e1rio:<\/span><\/p>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][dsm_embed_google_map address=”Episkey” _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][\/dsm_embed_google_map][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_contact_form email=”paloma.lopez@episkeymedical.com” custom_message=”Algu\u00e9m preencheu o formul\u00e1rio de contacto. ||et_pb_line_break_holder||Estes s\u00e3o os dados:||et_pb_line_break_holder||Nome: %%Nombre%%||et_pb_line_break_holder||Telefone: %%Tel\u00e9fono%%||et_pb_line_break_holder||E-mail: %%Email%%||et_pb_line_break_holder||Mensagem:||et_pb_line_break_holder||%%Mensaje%%” success_message=”Mensagem enviada com sucesso. Recebemos a sua solicita\u00e7\u00e3o. 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Consultoria em dispositivos m\u00e9dicosA melhor forma de garantir que os dispositivos m\u00e9dicos cumprem os requisitos regulamentares internacionais \u00e9 atrav\u00e9s de um servi\u00e7o de consultoria em dispositivos m\u00e9dicos.Os nossos servi\u00e7osOferecemos os melhores servi\u00e7os de consultoria em dispositivos m\u00e9dicos.Marca\u00e7\u00e3o CEpara dispositivos m\u00e9dicosOs nossos especialistas explicam-te como elaborar planos de desenvolvimento, de usabilidade e de valida\u00e7\u00e3o de software.Estrat\u00e9giaestrat\u00e9giaComercializa\u00e7\u00e3o […]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_et_pb_use_builder":"on","_et_pb_old_content":"","_et_gb_content_width":"","footnotes":""},"class_list":["post-18476","page","type-page","status-publish","hentry"],"yoast_head":"\nCasa - Episkey Medical<\/title>\n<meta name=\"description\" content=\"Casa en Episkey Medical\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/episkeymedical.com\/pt-pt\/\" \/>\n<meta property=\"og:locale\" content=\"pt_PT\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Casa - 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