{"id":39916,"date":"2013-09-11T12:45:00","date_gmt":"2013-09-11T16:45:00","guid":{"rendered":"http:\/\/1boringoldman.com\/?p=39916"},"modified":"2013-09-11T21:36:28","modified_gmt":"2013-09-12T01:36:28","slug":"eureka-i-hope","status":"publish","type":"post","link":"https:\/\/1boringoldman.com\/index.php\/2013\/09\/11\/eureka-i-hope\/","title":{"rendered":"eureka? I hope&#8230;"},"content":{"rendered":"<blockquote>\n<div align=\"center\" class=\"big\"><a href=\"http:\/\/www.pharmafile.com\/news\/180970\/uk-trial-rules-tightened#.UjB6lcJU5EI.twitter\" target=\"_blank\">UK trial rules tightened up<\/a><\/div>\n<div align=\"center\" class=\"big\"><strong><font color=\"#990000\">Pharmafile<\/font><\/strong><\/div>\n<div align=\"center\" class=\"middle\">by Adam Hill<\/div>\n<div align=\"center\" class=\"small\">Published on 11\/09\/13 at 02:03pm<\/div>\n<p align=\"justify\">Anyone wanting to conduct clinical trials in the UK will have to  register their research in order to receive a &lsquo;favourable ethical  opinion&rsquo; before they can begin, according to new rules to be introduced  at the end of the month. The Health Research Authority (HRA), whose remit is to protect and  promote the interests of patients and the public in health research, is  bringing in the plan from 30 September to ensure that UK trials are put  onto a public database.&nbsp; It means that from next month all studies should be registered before  the first patient is recruited: if this is not done within six weeks of  that first recruitment, the sponsor and investigator will fall foul of  the new rules. This new breach of good research practice will be added to the list  of those managed by Research Ethics Committees in the trial process.<\/p>\n<p align=\"justify\">The HRA is to consult with the medical devices sector with a view to imposing similar restrictions on it by March next year. We are fully committed to the principles of transparency in health  research,&rdquo; said HRA chief executive Janet Wisely. &ldquo;Including a  requirement for registration as a condition of the favourable ethical  opinion is a significant step towards this.&rdquo; It will be possible for those setting up trials to query the need for  registration but the HRA, created in December 2011 as a Special Health  Authority, warns that it &ldquo;does not&hellip;expect exceptions to be made&rdquo;.<\/p>\n<div align=\"justify\">The new ruling forms an interesting part of <a href=\"http:\/\/www.pharmafile.com\/news\/180960\/efpia-slams-ema-data-proposals\" target=\"_blank\">pharma&rsquo;s current transparency debate<\/a>  &#8211; not least because it does not only cover future research: the HRA  says it &ldquo;expects current and previous studies to be registered and  results to be put in the public domain&rdquo;. The HRA took on the activities of the National Research Ethics  Service, thus bringing together services previously provided by the  National Patient Safety Agency and some functions of the Strategic  Health Authorities.<\/div>\n<\/blockquote>\n<div align=\"justify\">If I read this correctly, it&#8217;s amazing news. It just popped up on Twitter from [you guessed it] Jack Friday of Pharmagossip&#8230; <\/div>\n<div align=\"justify\"><strong><font color=\"#200020\">Update<\/font><\/strong>: see <a target=\"_blank\" href=\"http:\/\/www.hra.nhs.uk\/EasySiteWeb\/GatewayLink.aspx?alId=179321\">this <\/a><\/div>\n","protected":false},"excerpt":{"rendered":"<p>UK trial rules tightened up Pharmafile by Adam Hill Published on 11\/09\/13 at 02:03pm Anyone wanting to conduct clinical trials in the UK will have to register their research in order to receive a &lsquo;favourable ethical opinion&rsquo; before they can begin, according to new rules to be introduced at the end of the month. The [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_bbp_topic_count":0,"_bbp_reply_count":0,"_bbp_total_topic_count":0,"_bbp_total_reply_count":0,"_bbp_voice_count":0,"_bbp_anonymous_reply_count":0,"_bbp_forum_subforum_count":0,"footnotes":""},"categories":[2],"tags":[],"class_list":["post-39916","post","type-post","status-publish","format-standard","hentry","category-politics"],"_links":{"self":[{"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/posts\/39916","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/comments?post=39916"}],"version-history":[{"count":5,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/posts\/39916\/revisions"}],"predecessor-version":[{"id":39930,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/posts\/39916\/revisions\/39930"}],"wp:attachment":[{"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/media?parent=39916"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/categories?post=39916"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/tags?post=39916"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}