{"id":12,"date":"2017-05-24T16:49:30","date_gmt":"2017-05-24T22:49:30","guid":{"rendered":"http:\/\/servidorabc.net\/medicaldevices\/?page_id=12"},"modified":"2019-08-12T22:17:32","modified_gmt":"2019-08-13T04:17:32","slug":"regulacion-sanitaria","status":"publish","type":"page","link":"https:\/\/crtmedicaldevices.com\/en\/regulacion-sanitaria\/","title":{"rendered":"REGULATORY AFFAIRS"},"content":{"rendered":"

[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”grid” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern” css=”.vc_custom_1497651662832{padding-top: 90px !important;padding-bottom: 90px !important;background-color: #8dd5ff !important;}” el_class=”centradocompleto”][vc_column width=”1\/2″][vc_single_image image=”337″ img_size=”full” alignment=”center” qode_css_animation=””][\/vc_column][vc_column width=”1\/2″][vc_column_text]<\/p>\n

We advice you throughout all the life cycle of your medical device; making it easier to obtain the registration(s) needed in the countries in which you\u2019re interested to distribute your medical device.<\/span><\/h2>\n

\u00a0<\/span><\/h2>\n

[\/vc_column_text][\/vc_column][\/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”grid” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern” css=”.vc_custom_1495731089463{padding-top: 65px !important;padding-bottom: 65px !important;background-color: #f4f4f4 !important;}”][vc_column width=”1\/3″][vc_column_text]<\/p>\n

Processes in Mexico (COFEPRIS)::<\/b><\/span><\/h3>\n

[\/vc_column_text][vc_empty_space]<\/i><\/span>[\/vc_column][vc_column width=”2\/3″][vc_column_text]<\/p>\n

    \n
  • Operation Notices and Sanitary Responsible<\/strong><\/li>\n
  • Dossiers\u2019<\/strong> preparation for New Health Registrations<\/strong> (classes I, II and III)<\/li>\n
  • Health Registrations Extensions (Renewals)<\/strong><\/li>\n
  • Health Registrations\u2019 Technical and Administrative Modifications<\/strong><\/li>\n
  • Compliance consulting of NOM 137 SSA1 2008<\/strong> \u2013 Medical Devices Labelling<\/li>\n<\/ul>\n

    [\/vc_column_text][\/vc_column][\/vc_row][vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”grid” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern” css=”.vc_custom_1495730996052{padding-top: 65px !important;padding-bottom: 65px !important;}”][vc_column]<\/i><\/span>[vc_empty_space][vc_column_text]<\/p>\n

    Processes in Latin America, Canada and Europe:<\/b><\/span><\/h3>\n

    [\/vc_column_text][vc_column_text]<\/p>\n

    Preparation of technical documentation to register medical devices<\/p>\n

    Consulting to comply with MDSAP audits<\/p>\n

    Preparation of technical documentation for obtaining CE mark<\/p>\n

    [\/vc_column_text][\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"

    [vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”grid” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern” css=”.vc_custom_1497651662832{padding-top: 90px !important;padding-bottom: 90px !important;background-color: #8dd5ff !important;}” el_class=”centradocompleto”][vc_column width=”1\/2″][vc_single_image image=”337″ img_size=”full” alignment=”center” qode_css_animation=””][\/vc_column][vc_column width=”1\/2″][vc_column_text] We advice you throughout all the life cycle of your medical device; making it easier to obtain the registration(s) needed in the countries…<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"full_width.php","meta":{"footnotes":""},"class_list":["post-12","page","type-page","status-publish","hentry"],"yoast_head":"\nREGULATORY AFFAIRS - Medical Devices<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/crtmedicaldevices.com\/es\/regulacion-sanitaria\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"REGULATORY AFFAIRS - Medical Devices\" \/>\n<meta property=\"og:description\" content=\"[vc_row css_animation=”” row_type=”row” use_row_as_full_screen_section=”no” type=”grid” angled_section=”no” text_align=”left” background_image_as_pattern=”without_pattern” css=”.vc_custom_1497651662832{padding-top: 90px !important;padding-bottom: 90px !important;background-color: #8dd5ff !important;}” el_class=”centradocompleto”][vc_column width=”1\/2″][vc_single_image image=”337″ img_size=”full” alignment=”center” qode_css_animation=””][\/vc_column][vc_column width=”1\/2″][vc_column_text] We advice you throughout all the life cycle of your medical device; 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