{"id":27273,"date":"2018-07-23T17:00:11","date_gmt":"2018-07-24T00:00:11","guid":{"rendered":"https:\/\/www.iths.org\/ctms\/?p=27273"},"modified":"2018-09-27T08:50:26","modified_gmt":"2018-09-27T15:50:26","slug":"introducing-clinical-research-support-regulatory-operations","status":"publish","type":"post","link":"https:\/\/www.iths.org\/ctms\/news\/introducing-clinical-research-support-regulatory-operations\/","title":{"rendered":"Introducing CRS Reg Ops"},"content":{"rendered":"<div class=\"wpb-content-wrapper\"><p>[vc_row css_animation=&#8221;&#8221; row_type=&#8221;row&#8221; use_row_as_full_screen_section=&#8221;no&#8221; type=&#8221;full_width&#8221; angled_section=&#8221;no&#8221; text_align=&#8221;left&#8221; background_image_as_pattern=&#8221;without_pattern&#8221;][vc_column][vc_column_text]<\/p>\n<h4><strong>CLINICAL RESEARCH SUPPORT REGULATORY OPERATIONS (CRS REG OPS) SUPPORTS STUDIES THAT DO NOT HAVE DEDICATED CLINICAL RESEARCH STAFF<\/strong><\/h4>\n<p>For these studies,\u00a0a central CRS team will enter the required protocol information, IRB status changes and other enrollment\u00a0information as applicable into the CTMS.\u00a0This will eliminate the need for CTMS training and data entry requirements for those staff with an otherwise limited need to work in the CTMS.<\/p>\n<p>For those research teams that fall in this category:[\/vc_column_text][\/vc_column][\/vc_row][vc_row css_animation=&#8221;&#8221; row_type=&#8221;row&#8221; use_row_as_full_screen_section=&#8221;no&#8221; type=&#8221;full_width&#8221; angled_section=&#8221;no&#8221; text_align=&#8221;left&#8221; background_image_as_pattern=&#8221;without_pattern&#8221;][vc_column][vc_column_text]<\/p>\n<h4>START<\/h4>\n<p>[\/vc_column_text]<div class=\"q_list circle animate_list\">\n\t<\/p>\n<ul>\n<li>Emailing <a href=\"mailto:submissions@fredhutch.org\" target=\"_blank\" rel=\"noopener noreferrer\">submissions@fredhutch.org<\/a>\u00a0when you have enrollments, if granular subject data is required.<\/li>\n<li>Copying <a href=\"mailto:submissions@fredhutch.org\" target=\"_blank\" rel=\"noopener noreferrer\">submissions@fredhutch.org<\/a>\u00a0when submitting modifications and renewals to the IRB.<\/li>\n<\/ul>\n<p><\/div>[\/vc_column][\/vc_row][vc_row css_animation=&#8221;&#8221; row_type=&#8221;row&#8221; use_row_as_full_screen_section=&#8221;no&#8221; type=&#8221;full_width&#8221; angled_section=&#8221;no&#8221; text_align=&#8221;left&#8221; background_image_as_pattern=&#8221;without_pattern&#8221;][vc_column][vc_column_text]<\/p>\n<h4>STOP<\/h4>\n<p>[\/vc_column_text]<div class=\"q_list circle animate_list\">\n\t<\/p>\n<ul>\n<li>Linking subjects in Epic (if previously applicable)<\/li>\n<li>Entering subjects into PATS (if previously applicable)<\/li>\n<\/ul>\n<p><\/div>[\/vc_column][\/vc_row][vc_row css_animation=&#8221;&#8221; row_type=&#8221;row&#8221; use_row_as_full_screen_section=&#8221;no&#8221; type=&#8221;full_width&#8221; angled_section=&#8221;no&#8221; text_align=&#8221;left&#8221; background_image_as_pattern=&#8221;without_pattern&#8221;][vc_column][vc_column_text]<\/p>\n<h4>CONTINUE<\/h4>\n<p>[\/vc_column_text]<div class=\"q_list circle animate_list\">\n\t<\/p>\n<ul>\n<li>Submitting modifications and renewals directly to the IRB<br \/>\n(CC: <a href=\"mailto:submissions@fredhutch.org\" target=\"_blank\" rel=\"noopener noreferrer\">submissions@fredhutch.org<\/a>)<\/li>\n<\/ul>\n<p><\/div>[\/vc_column][\/vc_row][vc_row css_animation=&#8221;&#8221; row_type=&#8221;row&#8221; use_row_as_full_screen_section=&#8221;no&#8221; type=&#8221;full_width&#8221; angled_section=&#8221;no&#8221; text_align=&#8221;left&#8221; background_image_as_pattern=&#8221;without_pattern&#8221;][vc_column][vc_separator type=&#8221;normal&#8221;][vc_column_text]If you have a question on whether or not your study should be under CRS Reg Ops, please contact the CTMS team at\u00a0<a href=\"mailto:ctmspm@uw.edu\">ctmspm@uw.edu<\/a>.[\/vc_column_text][\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"<p>The Clinical Research Support Regulatory Operations (CRS-RO) supports studies that do not have dedicated clinical research staff.<\/p>\n","protected":false},"author":1682,"featured_media":27280,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-27273","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-news"],"_links":{"self":[{"href":"https:\/\/www.iths.org\/ctms\/wp-json\/wp\/v2\/posts\/27273","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.iths.org\/ctms\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.iths.org\/ctms\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.iths.org\/ctms\/wp-json\/wp\/v2\/users\/1682"}],"replies":[{"embeddable":true,"href":"https:\/\/www.iths.org\/ctms\/wp-json\/wp\/v2\/comments?post=27273"}],"version-history":[{"count":10,"href":"https:\/\/www.iths.org\/ctms\/wp-json\/wp\/v2\/posts\/27273\/revisions"}],"predecessor-version":[{"id":27331,"href":"https:\/\/www.iths.org\/ctms\/wp-json\/wp\/v2\/posts\/27273\/revisions\/27331"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.iths.org\/ctms\/wp-json\/wp\/v2\/media\/27280"}],"wp:attachment":[{"href":"https:\/\/www.iths.org\/ctms\/wp-json\/wp\/v2\/media?parent=27273"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.iths.org\/ctms\/wp-json\/wp\/v2\/categories?post=27273"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.iths.org\/ctms\/wp-json\/wp\/v2\/tags?post=27273"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}