{"id":352,"date":"2017-08-14T15:39:57","date_gmt":"2017-08-14T07:39:57","guid":{"rendered":"https:\/\/credevo.com\/articles\/\/?p=352"},"modified":"2021-09-21T18:51:42","modified_gmt":"2021-09-21T10:51:42","slug":"why-your-clinical-trials-should-include-sites-in-romania","status":"publish","type":"post","link":"https:\/\/credevo.com\/articles\/2017\/08\/14\/why-your-clinical-trials-should-include-sites-in-romania\/","title":{"rendered":"Why Your Clinical Trials Should Include Sites in Romania?"},"content":{"rendered":"\n<p>The best&nbsp;reasons to conduct&nbsp;clinical trials in any country include the availability of patients, clarity of regulatory processes, willing and qualified investigators, and sound infrastructure at a reasonable cost. This is what you get if you conduct clinical trials in Romania. Let&#8217;s see this in greater detail.<\/p>\n\n\n\n<figure class=\"wp-block-image\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"548\" src=\"https:\/\/credevo.com\/articles\/\/wp-content\/uploads\/2017\/11\/Why_Your_Clinical_Trials_Should_Include_Sites_in_Romania_Credevo-1024x548.jpg\" alt=\"Why_Your_Clinical_Trials_Should_Include_Sites_in_Romania_Credevo\" class=\"wp-image-384\" srcset=\"https:\/\/credevo.com\/articles\/wp-content\/uploads\/2017\/11\/Why_Your_Clinical_Trials_Should_Include_Sites_in_Romania_Credevo-1024x548.jpg 1024w, https:\/\/credevo.com\/articles\/wp-content\/uploads\/2017\/11\/Why_Your_Clinical_Trials_Should_Include_Sites_in_Romania_Credevo-300x161.jpg 300w, https:\/\/credevo.com\/articles\/wp-content\/uploads\/2017\/11\/Why_Your_Clinical_Trials_Should_Include_Sites_in_Romania_Credevo-768x411.jpg 768w, https:\/\/credevo.com\/articles\/wp-content\/uploads\/2017\/11\/Why_Your_Clinical_Trials_Should_Include_Sites_in_Romania_Credevo-732x392.jpg 732w, https:\/\/credevo.com\/articles\/wp-content\/uploads\/2017\/11\/Why_Your_Clinical_Trials_Should_Include_Sites_in_Romania_Credevo-1140x610.jpg 1140w, https:\/\/credevo.com\/articles\/wp-content\/uploads\/2017\/11\/Why_Your_Clinical_Trials_Should_Include_Sites_in_Romania_Credevo.jpg 1920w\" sizes=\"(max-width: 1024px) 100vw, 1024px\" \/><\/figure>\n\n\n\n<h2 class=\"wp-block-heading\">Brief demography<\/h2>\n\n\n\n<ul class=\"wp-block-list\"><li>Romania is a&nbsp;sovereign state located in Southeastern Europe near Bulgaria, Ukraine, Hungary, Serbia, and Moldova.&nbsp;It&nbsp;is a developing country, part of the European Union, and is rapidly growing.<\/li><li>Romania has an economy predominantly based on services and is cementing its reputation as an industrious, educated, and ambitious region in many sectors.<\/li><li>Romania has one of the larger populations in the region with over 22 million. About 55% of the population resides in the urban areas with major concentrations in the cities of Iasi, Timisoara, Constanta, Cluj-Napoca, and Craiova.<\/li><\/ul>\n\n\n\n<h2 class=\"wp-block-heading\">Top 7 advantages of conducting clinical trials in Romania<\/h2>\n\n\n\n<p>The increased interest in Romania for clinical trials is not without sound reasons. Several factors provide great advantages to Romania&nbsp;in conducting clinical trials.<\/p>\n\n\n\n<ul class=\"wp-block-list\"><li><strong>Recruitment<\/strong><ul><li>High patient availability<\/li><li>Faster recruitment timelines<\/li><\/ul><\/li><\/ul>\n\n\n\n<ul class=\"wp-block-list\"><li><strong>Expertise<\/strong><ul><li>High standards of medical education,<\/li><li>Highly concentrated and specialized healthcare services,<\/li><li>Experienced personnel (including eCRF and IVRS solutions),<\/li><li>Relevant expertise<\/li><\/ul><\/li><\/ul>\n\n\n\n<ul class=\"wp-block-list\"><li><strong>Infrastructure<\/strong><ul><li>National infrastructure and environment,<\/li><li>Supportive infrastructure for clinical trials<\/li><\/ul><\/li><\/ul>\n\n\n\n<ul class=\"wp-block-list\"><li><strong>Cost<\/strong><ul><li>Cost-efficiency in operations<\/li><li>Great competitive cost per patient<\/li><\/ul><\/li><\/ul>\n\n\n\n<ul class=\"wp-block-list\"><li><strong>Quality<\/strong><ul><li>Good regulatory and protocol compliance with good-quality data<\/li><li>Sites certified by audits and inspections conducted by sponsor, regulatory or third parties.<\/li><\/ul><\/li><\/ul>\n\n\n\n<ul class=\"wp-block-list\"><li><strong>Time<\/strong><ul><li>Trial start-up times and requirements which are comparable with other EU countries,<\/li><li>Clarity about regulatory timelines<\/li><\/ul><\/li><\/ul>\n\n\n\n<ul class=\"wp-block-list\"><li><strong>Regulatory<\/strong><ul><li>Unambiguous regulatory conditions,<\/li><li>Synchronization with EU regulations<\/li><li>Almost all European guidelines and rules governing medicinal products in the EU have been transposed into national legislation in Romania<\/li><\/ul><\/li><\/ul>\n\n\n\n<h2 class=\"wp-block-heading\">Clinical trials status<\/h2>\n\n\n\n<p>Romania has a decent number of clinical trials to its share. The number of clinical trials is growing after economic changes in the late 20 century.<\/p>\n\n\n\n<ul class=\"wp-block-list\"><li>Total number of studies in Romania &#8211;&nbsp;<strong>2,618<\/strong> <a href=\"https:\/\/clinicaltrials.gov\/ct2\/results?cntry=RO&amp;Search=Apply&amp;age_v=&amp;gndr=&amp;type=&amp;rslt=\">(Clinicaltrials.gov)<\/a><\/li><li>Total number of recruiting studies in&nbsp;Romania &#8211; <b>265<\/b>&nbsp;<a href=\"https:\/\/clinicaltrials.gov\/ct2\/results?cntry=RO&amp;Search=Apply&amp;recrs=a&amp;age_v=&amp;gndr=&amp;type=&amp;rslt=\">(Clinicaltrials.gov)<\/a><\/li><\/ul>\n\n\n\n<p>Several clinical research organizations now include Romania as their region of work. Most of these are international, if not global, CROs and serve to connect Romania with other regions of clinical research.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Regulatory authority (RA)<\/h2>\n\n\n\n<p><strong>National Agency for Medicines and Medical Devices (NAMMD)<\/strong> serves as the regulatory authority governing the authorization of clinical trials in Romania.<\/p>\n\n\n\n<p>NAMMD grants clinical trial authorization to the sponsor or to the contracting research organization (CRO) acting on behalf of the sponsor.<\/p>\n\n\n\n<p>In some exceptions, in investigator-driven studies, the authorization can be granted to the investigator(s) initiating the trial, who will have certain attributions similar to a sponsor.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">The regulatory approval process<\/h2>\n\n\n\n<p><span style=\"font-weight: 400;\">The regulatory process for clinical trials approval in Romania is transparent and relatively fast. <\/span><\/p>\n\n\n\n<p><span style=\"font-weight: 400;\">Let&#8217;s discuss the regulatory process under three different kinds of approvals.<\/span><\/p>\n\n\n\n<ol class=\"wp-block-list\"><li><span style=\"font-weight: 400;\">Regulatory Authority (RA)<\/span><\/li><li><span style=\"font-weight: 400;\">Ethics Committee (IRB)<\/span><\/li><li><span style=\"font-weight: 400;\">Import Licence<\/span><\/li><\/ol>\n\n\n\n<h3 class=\"wp-block-heading\">Ethics Committee (IRB)<\/h3>\n\n\n\n<ul class=\"wp-block-list\"><li><span style=\"font-weight: 400;\">According to Ministry of Health Order 904\/2006 on the implementation of good practices in the performance of clinical studies, clinical trial activities are not permitted without a favorable opinion from the National Agency for Medicines and Medical Devices\u2019 ethics committee. <\/span><\/li><li><span style=\"font-weight: 400;\">This&nbsp;ethics body (National Ethics Commission) serves as the IRB arm for approval of clinical trials.<\/span><\/li><\/ul>\n\n\n\n<h3 class=\"wp-block-heading\">Import License<\/h3>\n\n\n\n<p>Import approval of the study drug is no longer necessary since the drugs are being imported based on the study approval.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Process of submission to RA &amp; IRB<\/h3>\n\n\n\n<ol class=\"wp-block-list\"><li><span style=\"font-weight: 400;\">The submission of the study documents can be done in parallel to both the competent regulatory authority (the National Medicines Agency) and the ethics body (National Ethics Commission), or the <\/span>applicant may request an IRB opinion before filing an authorization request..<\/li><li>According to National Agency for Medicines and Medical Devices Scientific Council Decision 2\/2014, clinical studies must be performed in authorized units only.<\/li><li>The unit authorization is valid for two years and may be extended upon request.<\/li><li>The scope of the authorization, as well as the necessary documentation, differs according to the type of trial the solicitant wishes to conduct (eg, authorization for clinical studies with therapeutic benefits, authorization for Phase I clinical trials, and authorization for bioequivalence clinical trials).<\/li><li>Applicant must notify RA&nbsp;by way of a signed letter of intent concerning the payment of the authorization fee and its intention to apply at least two weeks in advance.<\/li><li>Applicant must submit the documents listed in Annex 1 to Decision 6\/2014 in electronic form. These documents include a request for authorization, opinion of the ethics committee, information about the sponsor, and the medicine file.<\/li><li>It&#8217;s strongly recommended for applicants not to bring any important amendments to the initial request after 50 days following the payment of the authorization fee.<\/li><li>The signed approval order indicates the institution where the study will be conducted, and the principal investigator responsible for conducting it.<\/li><li>The authorization for clinical studies is valid for the period of the study. However, it loses validity if the study does not begin within one year of authorization being issued.<\/li><li>RA needs to be informed about the study\u2019s start date and any amendments to the study plan. Applicants must also notify RA when the study concludes.<\/li><\/ol>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img loading=\"lazy\" decoding=\"async\" width=\"960\" height=\"720\" src=\"https:\/\/credevo.com\/articles\/\/wp-content\/uploads\/2017\/11\/Clinical_Trial_Application_Romania_Credevo.jpg\" alt=\"Clinical_Trial_Application_Romania_Credevo\" class=\"wp-image-376\" srcset=\"https:\/\/credevo.com\/articles\/wp-content\/uploads\/2017\/11\/Clinical_Trial_Application_Romania_Credevo.jpg 960w, https:\/\/credevo.com\/articles\/wp-content\/uploads\/2017\/11\/Clinical_Trial_Application_Romania_Credevo-300x225.jpg 300w, https:\/\/credevo.com\/articles\/wp-content\/uploads\/2017\/11\/Clinical_Trial_Application_Romania_Credevo-768x576.jpg 768w, https:\/\/credevo.com\/articles\/wp-content\/uploads\/2017\/11\/Clinical_Trial_Application_Romania_Credevo-732x549.jpg 732w\" sizes=\"(max-width: 960px) 100vw, 960px\" \/><\/figure><\/div>\n\n\n\n<h2 class=\"wp-block-heading\">Clinical trial approval timelines<\/h2>\n\n\n\n<ol class=\"wp-block-list\"><li>The applicant will receive information about the validity of its request within 10 days of submission from RA.<\/li><li>In case of appropriate documentation is submitted, RA will issue an authorization within a maximum of 60 days.&nbsp;The examination of an application submitted to the regulatory authority in the proper format will not take more than 60 days.<\/li><li>In case of refusal, the applicant may request that the agency revise this within 30 days.<\/li><li>The ethics committee\u2019s opinion will also be issued within 60 days of a request.<\/li><\/ol>\n\n\n\n<h2 class=\"wp-block-heading\">The fee to conduct clinical trials in Romania<\/h2>\n\n\n\n<p>According to the authorization procedure for conducting clinical studies by the National Agency for Medicines and Medical Devices Scientific Council\u2019s Decision 6\/2014, the issuance of authorization for performing clinical studies is subject to the following fee structure:<\/p>\n\n\n\n<ul class=\"wp-block-list\"><li>\u20ac1,250 for new substances,<\/li><li>\u20ac1,000 for clinical investigation of medicines not authorized in Romania but authorized in other countries or authorized for marketing, when the study is conducted concerning aspects which fall outside the medicine\u2019s summary of characteristics,<\/li><li>\u20ac410 for studies performed on products authorized in Romania, used in conformity with their summary of characteristics, and<\/li><li>\u20ac600 for bioequivalence studies.<\/li><\/ul>\n\n\n\n<hr class=\"wp-block-separator\"\/>\n\n\n\n<h2 class=\"wp-block-heading\">Need Support for conducting your clinical trials in Romania or Have questions?<\/h2>\n\n\n\n<p>We&#8217;d love to help you conduct clinical trials in Romania.<\/p>\n\n\n\n<p>Provide your details below.<\/p>\n\n\n<div class=\"wpforms-container wpforms-container-full\" id=\"wpforms-4792\"><form id=\"wpforms-form-4792\" class=\"wpforms-validate wpforms-form\" data-formid=\"4792\" method=\"post\" enctype=\"multipart\/form-data\" action=\"\/articles\/wp-json\/wp\/v2\/posts\/352\" data-token=\"c3a2fca700f45dd9acb686726757d904\" data-token-time=\"1776640247\"><noscript class=\"wpforms-error-noscript\">Please enable JavaScript in your browser to complete this form.<\/noscript><div class=\"wpforms-field-container\"><div id=\"wpforms-4792-field_6-container\" class=\"wpforms-field wpforms-field-textarea\" data-field-id=\"6\"><label class=\"wpforms-field-label\" for=\"wpforms-4792-field_6\">What kind of support do you need in Romania? <span class=\"wpforms-required-label\">*<\/span><\/label><textarea id=\"wpforms-4792-field_6\" class=\"wpforms-field-medium wpforms-field-required\" name=\"wpforms[fields][6]\" required><\/textarea><\/div><div id=\"wpforms-4792-field_1-container\" class=\"wpforms-field wpforms-field-email\" data-field-id=\"1\"><label class=\"wpforms-field-label\" for=\"wpforms-4792-field_1\">What is your work email? <span class=\"wpforms-required-label\">*<\/span><\/label><input type=\"email\" id=\"wpforms-4792-field_1\" class=\"wpforms-field-medium wpforms-field-required\" name=\"wpforms[fields][1]\" spellcheck=\"false\" required><div class=\"wpforms-field-description\">Provide your work email, where we can contact you<\/div><\/div><\/div><!-- .wpforms-field-container --><div class=\"wpforms-field wpforms-field-hp\"><label for=\"wpforms-4792-field-hp\" class=\"wpforms-field-label\">Phone<\/label><input type=\"text\" name=\"wpforms[hp]\" id=\"wpforms-4792-field-hp\" class=\"wpforms-field-medium\"><\/div><div class=\"wpforms-recaptcha-container wpforms-is-recaptcha wpforms-is-recaptcha-type-v2\" ><div class=\"g-recaptcha\" data-sitekey=\"6LeaQRYTAAAAAPo7U8jnZJBUndxcS3f0E3Vijb2k\"><\/div><input type=\"text\" name=\"g-recaptcha-hidden\" class=\"wpforms-recaptcha-hidden\" style=\"position:absolute!important;clip:rect(0,0,0,0)!important;height:1px!important;width:1px!important;border:0!important;overflow:hidden!important;padding:0!important;margin:0!important;\" data-rule-recaptcha=\"1\"><\/div><div class=\"wpforms-submit-container\" ><input type=\"hidden\" name=\"wpforms[id]\" value=\"4792\"><input type=\"hidden\" name=\"page_title\" value=\"\"><input type=\"hidden\" name=\"page_url\" value=\"https:\/\/credevo.com\/articles\/wp-json\/wp\/v2\/posts\/352\"><input type=\"hidden\" name=\"url_referer\" value=\"\"><button type=\"submit\" name=\"wpforms[submit]\" id=\"wpforms-submit-4792\" class=\"wpforms-submit\" data-alt-text=\"Sending...\" data-submit-text=\"Submit\" aria-live=\"assertive\" value=\"wpforms-submit\">Submit<\/button><\/div><\/form><\/div>  <!-- .wpforms-container -->\n\n\n\n<hr class=\"wp-block-separator\"\/>\n\n\n\n<h4 class=\"wp-block-heading\">Click on the useful links below<\/h4>\n\n\n\n<ul class=\"wp-block-list\"><li><a href=\"https:\/\/credevo.com\/articles\/2017\/07\/17\/how-to-save-upto-80-of-cost-and-time-in-initiating-clinical-trials\/\">How To Save Upto 80% Of Cost And Time In Initiating Clinical Trials<\/a><\/li><li><a href=\"https:\/\/credevo.com\/articles\/2016\/10\/12\/finding-clinical-trials-to-work-upon-as-clinical-investigator\/\">Finding Clinical Trials to Work Upon as Clinical Investigator<\/a><\/li><\/ul>\n\n\n\n<h3 class=\"wp-block-heading\">References<\/h3>\n\n\n\n<ol class=\"wp-block-list\"><li><a href=\"http:\/\/synevo-centrallabs.eu\/media\/docs\/resources\/JCS_March_2014_Clinical_Trials_in_Romania.pdf\">http:\/\/synevo-centrallabs.eu\/media\/docs\/resources\/JCS_March_2014_Clinical_Trials_in_Romania.pdf<\/a><\/li><li><a href=\"http:\/\/www.jforcs.com\/wp-content\/uploads\/2015\/05\/09.-Romanias-Regulatory-Framework....pdf\">http:\/\/www.jforcs.com\/wp-content\/uploads\/2015\/05\/09.-Romanias-Regulatory-Framework&#8230;.pdf<\/a><\/li><li><a href=\"http:\/\/www.eurecnet.org\/information\/romania.html\">http:\/\/www.eurecnet.org\/information\/romania.html<\/a><\/li><li><a href=\"http:\/\/tangentdata.com\/clinical_trials_in_romania\">http:\/\/tangentdata.com\/clinical_trials_in_romania<\/a><\/li><li><a href=\"http:\/\/www.thelancet.com\/journals\/lancet\/article\/PIIS0140-6736(11)60372-3\/fulltext\">http:\/\/www.thelancet.com\/journals\/lancet\/article\/PIIS0140-6736(11)60372-3\/fulltext<\/a><\/li><li><a href=\"http:\/\/www.efgcp.eu\/Downloads\/EFGCPReportFiles\/Romania%20definitive.pdf\">http:\/\/www.efgcp.eu\/Downloads\/EFGCPReportFiles\/Romania%20definitive.pdf<\/a><\/li><li><a href=\"https:\/\/www.lexology.com\/library\/detail.aspx?g=b85fa44a-4fd8-480e-9b5c-ddca500815ea\">https:\/\/www.lexology.com\/library\/detail.aspx?g=b85fa44a-4fd8-480e-9b5c-ddca500815ea<\/a><\/li><\/ol>\n\n\n\n<p>Do you have any comments? please do not hesitate to put them below here.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>The best&nbsp;reasons to conduct&nbsp;clinical trials in any country include the availability of patients, clarity of regulatory processes, willing and qualified investigators, and sound infrastructure at a reasonable cost. This is what you get if you conduct clinical trials in Romania. Let&#8217;s see this in greater detail. Brief demography Romania is a&nbsp;sovereign state located in Southeastern [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":384,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"cybocfi_hide_featured_image":"","footnotes":""},"categories":[566,4],"tags":[267,541,68],"class_list":["post-352","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-clinical-development","category-regulatory","tag-clinical-trial","tag-nammd","tag-romania"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.6 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Why Your Clinical Trials Should Include Sites in Romania? | Credevo Articles<\/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:\/\/credevo.com\/articles\/2017\/08\/14\/why-your-clinical-trials-should-include-sites-in-romania\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Why Your Clinical Trials Should Include Sites in Romania? | Credevo Articles\" \/>\n<meta property=\"og:description\" content=\"The best&nbsp;reasons to conduct&nbsp;clinical trials in any country include the availability of patients, clarity of regulatory processes, willing and qualified investigators, and sound infrastructure at a reasonable cost. This is what you get if you conduct clinical trials in Romania. Let&#8217;s see this in greater detail. Brief demography Romania is a&nbsp;sovereign state located in Southeastern [&hellip;]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/credevo.com\/articles\/2017\/08\/14\/why-your-clinical-trials-should-include-sites-in-romania\/\" \/>\n<meta property=\"og:site_name\" content=\"Credevo Articles\" \/>\n<meta property=\"article:publisher\" content=\"https:\/\/www.facebook.com\/credevo\" \/>\n<meta property=\"article:published_time\" content=\"2017-08-14T07:39:57+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2021-09-21T10:51:42+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/credevo.com\/articles\/wp-content\/uploads\/2017\/11\/Why_Your_Clinical_Trials_Should_Include_Sites_in_Romania_Credevo.jpg\" \/>\n\t<meta property=\"og:image:width\" content=\"1920\" \/>\n\t<meta property=\"og:image:height\" content=\"1028\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/jpeg\" \/>\n<meta name=\"author\" content=\"Feasibility Team\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:creator\" content=\"@gocredevo\" \/>\n<meta name=\"twitter:site\" content=\"@gocredevo\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Feasibility Team\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"6 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\/\/credevo.com\/articles\/2017\/08\/14\/why-your-clinical-trials-should-include-sites-in-romania\/#article\",\"isPartOf\":{\"@id\":\"https:\/\/credevo.com\/articles\/2017\/08\/14\/why-your-clinical-trials-should-include-sites-in-romania\/\"},\"author\":{\"name\":\"Feasibility Team\",\"@id\":\"https:\/\/credevo.com\/articles\/#\/schema\/person\/eaf79e204cf3f6b11d8925cdd7adb3ed\"},\"headline\":\"Why Your Clinical Trials Should Include Sites in Romania?\",\"datePublished\":\"2017-08-14T07:39:57+00:00\",\"dateModified\":\"2021-09-21T10:51:42+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\/\/credevo.com\/articles\/2017\/08\/14\/why-your-clinical-trials-should-include-sites-in-romania\/\"},\"wordCount\":1200,\"publisher\":{\"@id\":\"https:\/\/credevo.com\/articles\/#organization\"},\"image\":{\"@id\":\"https:\/\/credevo.com\/articles\/2017\/08\/14\/why-your-clinical-trials-should-include-sites-in-romania\/#primaryimage\"},\"thumbnailUrl\":\"https:\/\/credevo.com\/articles\/wp-content\/uploads\/2017\/11\/Why_Your_Clinical_Trials_Should_Include_Sites_in_Romania_Credevo.jpg\",\"keywords\":[\"clinical trial\",\"NAMMD\",\"romania\"],\"articleSection\":[\"Clinical Development\",\"Regulatory\"],\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\/\/credevo.com\/articles\/2017\/08\/14\/why-your-clinical-trials-should-include-sites-in-romania\/\",\"url\":\"https:\/\/credevo.com\/articles\/2017\/08\/14\/why-your-clinical-trials-should-include-sites-in-romania\/\",\"name\":\"Why Your Clinical Trials Should Include Sites in Romania? 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