{"id":58724,"date":"2016-05-23T15:32:31","date_gmt":"2016-05-23T19:32:31","guid":{"rendered":"https:\/\/rarediseases.org\/nord-summit-2016\/"},"modified":"2016-05-23T15:32:31","modified_gmt":"2016-05-23T19:32:31","slug":"nord-summit-2016","status":"publish","type":"post","link":"https:\/\/rarediseases.org\/es\/nord-summit-2016\/","title":{"rendered":"NORD Summit 2016"},"content":{"rendered":"<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-26154 \" src=\"https:\/\/rarediseases.org\/wp-content\/uploads\/2016\/05\/RareSummit2016_live-1024x399.jpg\" alt=\"RareSummit2016_live\" width=\"529\" height=\"206\" \/><\/p>\n<p>Save the date for the 2016 NORD Summit! Attendees can look forward to:<\/p>\n<ul>\n<li>Timely Topics\n<ul>\n<li>Sessions on genetic innovation, collaborations across borders, reimbursement, pricing and access, off-label concerns, driving progress through policy and more.<\/li>\n<\/ul>\n<\/li>\n<li>Inspiring Perspectives\n<ul>\n<li>Hear from manufacturers, patients, advocates, legislative and regulatory leaders, academics, researchers and more as they trail-blaze the road ahead in diagnosis, treatment and access for patients<\/li>\n<\/ul>\n<\/li>\n<li>Breakthrough Conversations\n<ul>\n<li>Immerse yourself in networking with hundreds of stakeholders all dedicated to creating meaningful change in the lives of rare disease patients<\/li>\n<\/ul>\n<\/li>\n<li>One of a Kind Experience\n<ul>\n<li>The meeting with the highest level of FDA involvement, and the only place where the who&#8217;s who in rare diseases convene to network and build partnerships<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<p><strong>Learn more about the event. <a href=\"https:\/\/nordsummit.org\" target=\"_blank\" rel=\"noopener nofollow\">Visit our website here.<\/a>\u00a0<\/strong><\/p>\n","protected":false},"excerpt":{"rendered":"<p>NORD&#8217;s Rare Diseases and Orphan Products Breakthrough Summit will be held in Arlington, VA October 17-18<\/p>\n","protected":false},"author":1,"featured_media":12199,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_relevanssi_hide_post":"","_relevanssi_hide_content":"","_relevanssi_pin_for_all":"","_relevanssi_pin_keywords":"","_relevanssi_unpin_keywords":"","_relevanssi_related_keywords":"","_relevanssi_related_include_ids":"","_relevanssi_related_exclude_ids":"","_relevanssi_related_no_append":"","_relevanssi_related_not_related":"","_relevanssi_related_posts":"","_relevanssi_noindex_reason":"","_price":"","_stock":"","_tribe_ticket_header":"","_tribe_default_ticket_provider":"","_tribe_ticket_capacity":"","_ticket_start_date":"","_ticket_end_date":"","_tribe_ticket_show_description":"","_tribe_ticket_show_not_going":false,"_tribe_ticket_use_global_stock":"","_tribe_ticket_global_stock_level":"","_global_stock_mode":"","_global_stock_cap":"","_tribe_rsvp_for_event":"","_tribe_ticket_going_count":"","_tribe_ticket_not_going_count":"","_tribe_tickets_list":"[]","_tribe_ticket_has_attendee_info_fields":false,"footnotes":""},"categories":[232,503,190,662,210,192,193],"tags":[253,1128,244,926,265,200,315,643,1127,383,1129],"class_list":["post-58724","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-advocacy","category-events","category-featured-news","category-get-involved","category-industry","category-patients-members","category-research","tag-advocacy","tag-arlington","tag-fda","tag-industry","tag-nih","tag-nord-summit","tag-rare-disease","tag-rare-diseases-and-orphan-products-breakthrough-summit","tag-rare-summit","tag-research","tag-virginia"],"acf":[],"_links":{"self":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58724","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/comments?post=58724"}],"version-history":[{"count":0,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58724\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media\/12199"}],"wp:attachment":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media?parent=58724"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/categories?post=58724"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/tags?post=58724"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}