{"id":11173,"date":"2025-09-25T14:30:00","date_gmt":"2025-09-25T06:30:00","guid":{"rendered":"https:\/\/credevo.com\/articles\/?p=11173"},"modified":"2025-09-08T12:05:27","modified_gmt":"2025-09-08T04:05:27","slug":"planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps","status":"publish","type":"post","link":"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/","title":{"rendered":"Planning Clinical Trials In Japan? Here\u2019s How To Ship Your Ancillaries &amp; Non-IMPs"},"content":{"rendered":"\n<p>If you&#8217;re planning a clinical trial in Japan, one of the most important (and often overlooked) aspects is how to properly ship your ancillary supplies and non-IMPs. In particular, lab kits, diagnostic devices, and other materials may be required. Therefore<strong>,<\/strong> navigating import requirements is not always straightforward. With strict regulations and detailed customs procedures, a small mistake can lead to major delays.\u00a0<\/p>\n\n\n\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"576\" src=\"https:\/\/credevo.com\/articles\/wp-content\/uploads\/2025\/09\/ClinicalTrials_Japan_Ship_Ancillaries__Non-IMPs_Credevo-1-1024x576.png\" alt=\"planning a clinical trial in Japan\" class=\"wp-image-11176\" srcset=\"https:\/\/credevo.com\/articles\/wp-content\/uploads\/2025\/09\/ClinicalTrials_Japan_Ship_Ancillaries__Non-IMPs_Credevo-1-1024x576.png 1024w, https:\/\/credevo.com\/articles\/wp-content\/uploads\/2025\/09\/ClinicalTrials_Japan_Ship_Ancillaries__Non-IMPs_Credevo-1-300x169.png 300w, https:\/\/credevo.com\/articles\/wp-content\/uploads\/2025\/09\/ClinicalTrials_Japan_Ship_Ancillaries__Non-IMPs_Credevo-1-768x432.png 768w, https:\/\/credevo.com\/articles\/wp-content\/uploads\/2025\/09\/ClinicalTrials_Japan_Ship_Ancillaries__Non-IMPs_Credevo-1-1536x864.png 1536w, https:\/\/credevo.com\/articles\/wp-content\/uploads\/2025\/09\/ClinicalTrials_Japan_Ship_Ancillaries__Non-IMPs_Credevo-1-2048x1152.png 2048w, https:\/\/credevo.com\/articles\/wp-content\/uploads\/2025\/09\/ClinicalTrials_Japan_Ship_Ancillaries__Non-IMPs_Credevo-1-732x412.png 732w, https:\/\/credevo.com\/articles\/wp-content\/uploads\/2025\/09\/ClinicalTrials_Japan_Ship_Ancillaries__Non-IMPs_Credevo-1-1140x641.png 1140w\" sizes=\"(max-width: 1024px) 100vw, 1024px\" \/><\/figure>\n\n\n\n<p>In this article, we\u2019ll walk you through what you need to know about shipping non-IMPs and ancillaries to Japan, including regulatory tips, documentation requirements, and practical advice to help your trial run smoothly.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Regulatory &amp; compliance<\/h2>\n\n\n\n<h4 class=\"wp-block-heading\">Navigating Japan\u2019s import regulations for clinical trials<\/h4>\n\n\n\n<p>Japan enforces stringent regulations when it comes to importing materials related to clinical research. Whether or not your shipment includes pharmaceutical products, its role in a clinical trial can place it under regulatory scrutiny. This includes non-IMPs and ancillary items like medical devices, collection kits, or diagnostic supplies.<\/p>\n\n\n\n<p>To comply, you\u2019ll need a solid understanding of required documents, such as study protocols, item specifications, and intended use. Missteps like incomplete paperwork or incorrect classification can lead to delays, fines, or customs rejection.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\">PMDA Guidelines: Key points before shipping<\/h4>\n\n\n\n<p>The <a href=\"https:\/\/www.pmda.go.jp\/english\/\" target=\"_blank\" rel=\"noreferrer noopener\">Pharmaceuticals and Medical Devices Agency (PMDA)<\/a> oversees all clinical trial activity in Japan. While non-IMPs and ancillaries don\u2019t go through the same approval process as IMPs, they must still meet GCP and GDP standards.<\/p>\n\n\n\n<p>Key expectations include:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Demonstrating the item\u2019s role in the clinical trial<\/li>\n\n\n\n<li>Ensuring that the import supports patient safety and ethical standards<\/li>\n\n\n\n<li>Aligning documentation with study filings<\/li>\n\n\n\n<li>Clearly defining the responsibilities of your Importer of Record (IOR)<\/li>\n<\/ul>\n\n\n\n<p>Non-compliance can bring serious consequences, delays, regulatory queries, or even project disruption.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\">IOR\/EOR compliance for ancillary supplies<\/h4>\n\n\n\n<p>Appointing a qualified Importer of Record (IOR) and Exporter of Record (EOR) is not just helpful, it\u2019s essential. These entities ensure your materials meet all Japanese customs and regulatory requirements.<\/p>\n\n\n\n<p>Their responsibilities include:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Filing accurate declarations with customs<\/li>\n\n\n\n<li>Correctly classifying goods under HS codes<\/li>\n\n\n\n<li>Coordinating with PMDA and customs officials as needed<\/li>\n\n\n\n<li>Keeping clear documentation and audit trails<\/li>\n<\/ul>\n\n\n\n<p>For clinical trials, it\u2019s especially important to work with an IOR\/EOR experienced in research logistics. <em>Therefore,<\/em> avoid relying on general trade providers to ensure nothing gets lost in translation.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Logistics &amp; documentation<\/h2>\n\n\n\n<h4 class=\"wp-block-heading\">What documents do you need?<\/h4>\n\n\n\n<p>Smooth customs clearance depends on comprehensive and accurate documentation. Required documents typically include product details, clinical trial documents, and relevant technical information. <strong>However,<\/strong> the exact requirements will become clear <strong>once<\/strong> the type of product to be shipped is well understood.<\/p>\n\n\n\n<p>Would you like to know which documents are required to import your clinical trial ancillaries, non-IMPs, or medical devices into Japan? Share the shipment details through the form below, and we\u2019ll provide you with the relevant documentation and compliance guidance.<\/p>\n\n\n\n<p>Errors or omissions in these documents are among the most common causes of customs delays.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\">Labeling &amp; packaging essentials<\/h4>\n\n\n\n<p>Japan has specific rules for how trial materials should be labeled and packaged, even non-IMPs and ancillaries. Mistakes here can lead to customs holds or rejections.<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>Language:<\/strong> Labels should be in English and\/or Japanese<\/li>\n\n\n\n<li><strong>Label Contents:<\/strong> Include product name, lot number, expiry date, and storage instructions<\/li>\n\n\n\n<li><strong>Usage Statement:<\/strong> \u201cFor Clinical Trial Use Only\u201d is often required<\/li>\n\n\n\n<li><strong>Cold Chain:<\/strong> If temperature-sensitive, include proper loggers and markings<\/li>\n\n\n\n<li><strong>Packaging:<\/strong> Must be secure, tamper-proof, and clearly organized<\/li>\n<\/ul>\n\n\n\n<h4 class=\"wp-block-heading\">Avoiding shipment Delays: What to watch out for<\/h4>\n\n\n\n<p>Some of the most common shipment problems include:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Documentation that doesn\u2019t match shipment contents<\/li>\n\n\n\n<li>Lack of clarity on the IOR\/EOR role<\/li>\n\n\n\n<li>Incorrect HS code classification<\/li>\n\n\n\n<li>Missing import licenses for medical devices<\/li>\n\n\n\n<li>PMDA filing misalignment<\/li>\n<\/ul>\n\n\n\n<p>How to prevent them:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Work with an IOR\/EOR that understands Japan\u2019s clinical trial requirements<\/li>\n\n\n\n<li>Double-check your paperwork before shipping<\/li>\n\n\n\n<li>Communicate regularly with your logistics team and receiving sites<br>Prepare contingency plans for customs queries<\/li>\n<\/ul>\n\n\n\n<h2 class=\"wp-block-heading\">Role of IOR\/EOR in planning a clinical trial in Japan<\/h2>\n\n\n\n<p>As we detailed in our <a href=\"https:\/\/credevo.com\/articles\/2023\/03\/25\/the-role-of-ior-eor-services-in-optimizing-clinical-trials-in-japan\/\" target=\"_blank\" rel=\"noreferrer noopener\">article<\/a>, having the right IOR and EOR partner is critical for ensuring clinical trial shipments to Japan are smooth and compliant, especially if your organization doesn\u2019t have a local office.<\/p>\n\n\n\n<p>A knowledgeable IOR\/EOR can:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Navigate regulatory hurdles<\/li>\n\n\n\n<li>Submit correct import\/export declarations<\/li>\n\n\n\n<li>Keep your study on schedule<\/li>\n<\/ul>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p><strong>For more details<\/strong>, refer to our <a href=\"https:\/\/credevo.com\/articles\/2023\/03\/25\/the-role-of-ior-eor-services-in-optimizing-clinical-trials-in-japan\/\" target=\"_blank\" rel=\"noreferrer noopener\">article<\/a> on IOR\/EOR roles in Japan\u2019s clinical trial logistics.<\/p>\n<\/blockquote>\n\n\n\n<h2 class=\"wp-block-heading\">Practical insights<\/h2>\n\n\n\n<h4 class=\"wp-block-heading\">Plan ahead to stay on track<\/h4>\n\n\n\n<p>Timing is everything when it comes to clinical trial logistics. To avoid delays:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Start planning 3\u20135 weeks in advance<\/li>\n\n\n\n<li>Coordinate with local sites and regulatory teams<\/li>\n\n\n\n<li>Account for holidays like Golden Week or New Year<\/li>\n\n\n\n<li>Notify your IOR\/EOR early so they can prepare<\/li>\n<\/ul>\n\n\n\n<h4 class=\"wp-block-heading\">Real-world challenges &amp; how to solve them<\/h4>\n\n\n\n<p>In past projects, we\u2019ve seen:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Shipments held due to missing \u201cClinical Use Only\u201d labels<\/li>\n\n\n\n<li>Delays from using IORs who are unfamiliar with trial documentation<\/li>\n\n\n\n<li>Confusion over HS code classification resulting in rejections<\/li>\n<\/ul>\n\n\n\n<p>These issues were resolved by involving IOR\/EOR partners early and conducting pre-shipment reviews.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\">Tips for smooth deliveries<\/h4>\n\n\n\n<p>Here\u2019s how to ensure your shipments reach Japanese clinical sites without a hitch:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Confirm the IOR\/EOR\u2019s readiness early<\/li>\n\n\n\n<li>Use logistics providers familiar with Japanese clinical trials<\/li>\n\n\n\n<li>Prepare complete and accurate paperwork<\/li>\n\n\n\n<li>Double-check labeling and packaging for local standards<\/li>\n\n\n\n<li>Keep your sites informed and ready to receive shipments<\/li>\n\n\n\n<li>Build extra time into your logistics schedule<\/li>\n<\/ul>\n\n\n\n<h2 class=\"wp-block-heading\">Conclusion for planning a clinical trial in Japan<\/h2>\n\n\n\n<p>Successfully shipping ancillaries and non-IMPs for clinical trials in Japan requires careful planning, precise documentation, and close coordination with experienced IOR\/EOR partners. By preparing early, aligning with PMDA guidelines, and ensuring compliance at every step, you can minimize delays and keep your study on track. Thoughtful logistics management is not just about moving goods; it\u2019s about safeguarding your trial\u2019s timeline and success.<\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<h2 class=\"wp-block-heading\">Are you still facing challenges or have specific questions?<\/h2>\n\n\n\n<p>Are you struggling with complex documentation, navigating Japanese customs regulations, or perhaps facing unexpected delays in shipping ancillaries and medical devices for your clinical trials? If so<strong>,<\/strong> and if you want to ensure everything goes smoothly, fill out the form below. Our experienced team will connect with you to address your concerns and provide clear, step-by-step guidance for a compliant and efficient import process.<\/p>\n\n\n<div class=\"wpforms-container wpforms-container-full\" id=\"wpforms-11198\"><form id=\"wpforms-form-11198\" class=\"wpforms-validate wpforms-form\" data-formid=\"11198\" method=\"post\" enctype=\"multipart\/form-data\" action=\"\/articles\/wp-json\/wp\/v2\/posts\/11173\" data-token=\"5a3c649dafe337d3cd2ce8c5267eb0f4\" data-token-time=\"1775397596\"><noscript class=\"wpforms-error-noscript\">Please enable JavaScript in your browser to complete this form.<\/noscript><div class=\"wpforms-field-container\"><div id=\"wpforms-11198-field_7-container\" class=\"wpforms-field wpforms-field-textarea\" data-field-id=\"7\"><label class=\"wpforms-field-label\" for=\"wpforms-11198-field_7\">Provide your requirement details here <span class=\"wpforms-required-label\">*<\/span><\/label><textarea id=\"wpforms-11198-field_7\" class=\"wpforms-field-medium wpforms-field-required\" name=\"wpforms[fields][7]\" required><\/textarea><div class=\"wpforms-field-description\">Provide brief info about what kind of support you are looking for<\/div><\/div><div id=\"wpforms-11198-field_8-container\" class=\"wpforms-field wpforms-field-text\" data-field-id=\"8\"><label class=\"wpforms-field-label\" for=\"wpforms-11198-field_8\">Provide your Company\/Organization name <span class=\"wpforms-required-label\">*<\/span><\/label><input type=\"text\" id=\"wpforms-11198-field_8\" class=\"wpforms-field-medium wpforms-field-required\" name=\"wpforms[fields][8]\" required><\/div><div id=\"wpforms-11198-field_1-container\" class=\"wpforms-field wpforms-field-email\" data-field-id=\"1\"><label class=\"wpforms-field-label\" for=\"wpforms-11198-field_1\">What is your work email? <span class=\"wpforms-required-label\">*<\/span><\/label><input type=\"email\" id=\"wpforms-11198-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-11198-field-hp\" class=\"wpforms-field-label\">Website<\/label><input type=\"text\" name=\"wpforms[hp]\" id=\"wpforms-11198-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=\"11198\"><input type=\"hidden\" name=\"page_title\" value=\"\"><input type=\"hidden\" name=\"page_url\" value=\"https:\/\/credevo.com\/articles\/wp-json\/wp\/v2\/posts\/11173\"><input type=\"hidden\" name=\"url_referer\" value=\"\"><button type=\"submit\" name=\"wpforms[submit]\" id=\"wpforms-submit-11198\" 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 has-alpha-channel-opacity\"\/>\n","protected":false},"excerpt":{"rendered":"<p>If you&#8217;re planning a clinical trial in Japan, one of the most important (and often overlooked) aspects is how to properly ship your ancillary supplies and non-IMPs. In particular, lab kits, diagnostic devices, and other materials may be required. Therefore, navigating import requirements is not always straightforward. With strict regulations and detailed customs procedures, a [&hellip;]<\/p>\n","protected":false},"author":6,"featured_media":11176,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"cybocfi_hide_featured_image":"yes","footnotes":""},"categories":[12],"tags":[714,45,149],"class_list":["post-11173","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-clinical-trial","tag-ancillaries","tag-clinicaltrials","tag-japan"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.6 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Planning a clinical trial in Japan<\/title>\n<meta name=\"description\" content=\"Planning clinical trial in Japan requires compliance. Discover how to ship ancillaries &amp; non-IMPs with ease.\" \/>\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\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Planning a clinical trial in Japan\" \/>\n<meta property=\"og:description\" content=\"Planning clinical trial in Japan requires compliance. Discover how to ship ancillaries &amp; non-IMPs with ease.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/\" \/>\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=\"2025-09-25T06:30:00+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2025-09-08T04:05:27+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/credevo.com\/articles\/wp-content\/uploads\/2025\/09\/ClinicalTrials_Japan_Ship_Ancillaries__Non-IMPs_Credevo-1-1024x576.png\" \/>\n\t<meta property=\"og:image:width\" content=\"1024\" \/>\n\t<meta property=\"og:image:height\" content=\"576\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/png\" \/>\n<meta name=\"author\" content=\"Trial Support\" \/>\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=\"Trial Support\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"5 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/#article\",\"isPartOf\":{\"@id\":\"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/\"},\"author\":{\"name\":\"Trial Support\",\"@id\":\"https:\/\/credevo.com\/articles\/#\/schema\/person\/ec7c79ef32c15761f618503e81d76523\"},\"headline\":\"Planning Clinical Trials In Japan? Here\u2019s How To Ship Your Ancillaries &amp; Non-IMPs\",\"datePublished\":\"2025-09-25T06:30:00+00:00\",\"dateModified\":\"2025-09-08T04:05:27+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/\"},\"wordCount\":1049,\"publisher\":{\"@id\":\"https:\/\/credevo.com\/articles\/#organization\"},\"image\":{\"@id\":\"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/#primaryimage\"},\"thumbnailUrl\":\"https:\/\/credevo.com\/articles\/wp-content\/uploads\/2025\/09\/ClinicalTrials_Japan_Ship_Ancillaries__Non-IMPs_Credevo-1.png\",\"keywords\":[\"Ancillaries\",\"clinicaltrials\",\"Japan\"],\"articleSection\":[\"clinical trial\"],\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/\",\"url\":\"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/\",\"name\":\"Planning a clinical trial in Japan\",\"isPartOf\":{\"@id\":\"https:\/\/credevo.com\/articles\/#website\"},\"primaryImageOfPage\":{\"@id\":\"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/#primaryimage\"},\"image\":{\"@id\":\"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/#primaryimage\"},\"thumbnailUrl\":\"https:\/\/credevo.com\/articles\/wp-content\/uploads\/2025\/09\/ClinicalTrials_Japan_Ship_Ancillaries__Non-IMPs_Credevo-1.png\",\"datePublished\":\"2025-09-25T06:30:00+00:00\",\"dateModified\":\"2025-09-08T04:05:27+00:00\",\"description\":\"Planning clinical trial in Japan requires compliance. Discover how to ship ancillaries & non-IMPs with ease.\",\"breadcrumb\":{\"@id\":\"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\/\/credevo.com\/articles\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Planning Clinical Trials In Japan? Here\u2019s How To Ship Your Ancillaries &amp; Non-IMPs\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\/\/credevo.com\/articles\/#website\",\"url\":\"https:\/\/credevo.com\/articles\/\",\"name\":\"Credevo\",\"description\":\"\",\"publisher\":{\"@id\":\"https:\/\/credevo.com\/articles\/#organization\"},\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/credevo.com\/articles\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"},{\"@type\":\"Organization\",\"@id\":\"https:\/\/credevo.com\/articles\/#organization\",\"name\":\"Credevo Pte. Ltd.\",\"url\":\"https:\/\/credevo.com\/articles\/\",\"logo\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\/\/credevo.com\/articles\/#\/schema\/logo\/image\/\",\"url\":\"https:\/\/credevo.com\/articles\/wp-content\/uploads\/2021\/04\/CREDEVO-HORIZONTAL.jpg\",\"contentUrl\":\"https:\/\/credevo.com\/articles\/wp-content\/uploads\/2021\/04\/CREDEVO-HORIZONTAL.jpg\",\"width\":320,\"height\":119,\"caption\":\"Credevo Pte. Ltd.\"},\"image\":{\"@id\":\"https:\/\/credevo.com\/articles\/#\/schema\/logo\/image\/\"},\"sameAs\":[\"https:\/\/www.facebook.com\/credevo\",\"https:\/\/x.com\/gocredevo\",\"https:\/\/www.instagram.com\/credevo_official\/\",\"https:\/\/www.linkedin.com\/company\/credevo\"]},{\"@type\":\"Person\",\"@id\":\"https:\/\/credevo.com\/articles\/#\/schema\/person\/ec7c79ef32c15761f618503e81d76523\",\"name\":\"Trial Support\",\"image\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\/\/credevo.com\/articles\/#\/schema\/person\/image\/\",\"url\":\"https:\/\/secure.gravatar.com\/avatar\/782274a75715e6d8bbd2447abf2c1a4c?s=96&d=mm&r=g\",\"contentUrl\":\"https:\/\/secure.gravatar.com\/avatar\/782274a75715e6d8bbd2447abf2c1a4c?s=96&d=mm&r=g\",\"caption\":\"Trial Support\"},\"url\":\"https:\/\/credevo.com\/articles\/author\/regulatory\/\"}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Planning a clinical trial in Japan","description":"Planning clinical trial in Japan requires compliance. Discover how to ship ancillaries & non-IMPs with ease.","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/","og_locale":"en_US","og_type":"article","og_title":"Planning a clinical trial in Japan","og_description":"Planning clinical trial in Japan requires compliance. Discover how to ship ancillaries & non-IMPs with ease.","og_url":"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/","og_site_name":"Credevo Articles","article_publisher":"https:\/\/www.facebook.com\/credevo","article_published_time":"2025-09-25T06:30:00+00:00","article_modified_time":"2025-09-08T04:05:27+00:00","og_image":[{"width":1024,"height":576,"url":"https:\/\/credevo.com\/articles\/wp-content\/uploads\/2025\/09\/ClinicalTrials_Japan_Ship_Ancillaries__Non-IMPs_Credevo-1-1024x576.png","type":"image\/png"}],"author":"Trial Support","twitter_card":"summary_large_image","twitter_creator":"@gocredevo","twitter_site":"@gocredevo","twitter_misc":{"Written by":"Trial Support","Est. reading time":"5 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/#article","isPartOf":{"@id":"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/"},"author":{"name":"Trial Support","@id":"https:\/\/credevo.com\/articles\/#\/schema\/person\/ec7c79ef32c15761f618503e81d76523"},"headline":"Planning Clinical Trials In Japan? Here\u2019s How To Ship Your Ancillaries &amp; Non-IMPs","datePublished":"2025-09-25T06:30:00+00:00","dateModified":"2025-09-08T04:05:27+00:00","mainEntityOfPage":{"@id":"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/"},"wordCount":1049,"publisher":{"@id":"https:\/\/credevo.com\/articles\/#organization"},"image":{"@id":"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/#primaryimage"},"thumbnailUrl":"https:\/\/credevo.com\/articles\/wp-content\/uploads\/2025\/09\/ClinicalTrials_Japan_Ship_Ancillaries__Non-IMPs_Credevo-1.png","keywords":["Ancillaries","clinicaltrials","Japan"],"articleSection":["clinical trial"],"inLanguage":"en-US"},{"@type":"WebPage","@id":"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/","url":"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/","name":"Planning a clinical trial in Japan","isPartOf":{"@id":"https:\/\/credevo.com\/articles\/#website"},"primaryImageOfPage":{"@id":"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/#primaryimage"},"image":{"@id":"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/#primaryimage"},"thumbnailUrl":"https:\/\/credevo.com\/articles\/wp-content\/uploads\/2025\/09\/ClinicalTrials_Japan_Ship_Ancillaries__Non-IMPs_Credevo-1.png","datePublished":"2025-09-25T06:30:00+00:00","dateModified":"2025-09-08T04:05:27+00:00","description":"Planning clinical trial in Japan requires compliance. Discover how to ship ancillaries & non-IMPs with ease.","breadcrumb":{"@id":"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/credevo.com\/articles\/2025\/09\/25\/planning-clinical-trials-in-japan-heres-how-to-ship-your-ancillaries-non-imps\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/credevo.com\/articles\/"},{"@type":"ListItem","position":2,"name":"Planning Clinical Trials In Japan? Here\u2019s How To Ship Your Ancillaries &amp; Non-IMPs"}]},{"@type":"WebSite","@id":"https:\/\/credevo.com\/articles\/#website","url":"https:\/\/credevo.com\/articles\/","name":"Credevo","description":"","publisher":{"@id":"https:\/\/credevo.com\/articles\/#organization"},"potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/credevo.com\/articles\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"en-US"},{"@type":"Organization","@id":"https:\/\/credevo.com\/articles\/#organization","name":"Credevo Pte. Ltd.","url":"https:\/\/credevo.com\/articles\/","logo":{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/credevo.com\/articles\/#\/schema\/logo\/image\/","url":"https:\/\/credevo.com\/articles\/wp-content\/uploads\/2021\/04\/CREDEVO-HORIZONTAL.jpg","contentUrl":"https:\/\/credevo.com\/articles\/wp-content\/uploads\/2021\/04\/CREDEVO-HORIZONTAL.jpg","width":320,"height":119,"caption":"Credevo Pte. Ltd."},"image":{"@id":"https:\/\/credevo.com\/articles\/#\/schema\/logo\/image\/"},"sameAs":["https:\/\/www.facebook.com\/credevo","https:\/\/x.com\/gocredevo","https:\/\/www.instagram.com\/credevo_official\/","https:\/\/www.linkedin.com\/company\/credevo"]},{"@type":"Person","@id":"https:\/\/credevo.com\/articles\/#\/schema\/person\/ec7c79ef32c15761f618503e81d76523","name":"Trial Support","image":{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/credevo.com\/articles\/#\/schema\/person\/image\/","url":"https:\/\/secure.gravatar.com\/avatar\/782274a75715e6d8bbd2447abf2c1a4c?s=96&d=mm&r=g","contentUrl":"https:\/\/secure.gravatar.com\/avatar\/782274a75715e6d8bbd2447abf2c1a4c?s=96&d=mm&r=g","caption":"Trial Support"},"url":"https:\/\/credevo.com\/articles\/author\/regulatory\/"}]}},"_links":{"self":[{"href":"https:\/\/credevo.com\/articles\/wp-json\/wp\/v2\/posts\/11173"}],"collection":[{"href":"https:\/\/credevo.com\/articles\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/credevo.com\/articles\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/credevo.com\/articles\/wp-json\/wp\/v2\/users\/6"}],"replies":[{"embeddable":true,"href":"https:\/\/credevo.com\/articles\/wp-json\/wp\/v2\/comments?post=11173"}],"version-history":[{"count":6,"href":"https:\/\/credevo.com\/articles\/wp-json\/wp\/v2\/posts\/11173\/revisions"}],"predecessor-version":[{"id":11205,"href":"https:\/\/credevo.com\/articles\/wp-json\/wp\/v2\/posts\/11173\/revisions\/11205"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/credevo.com\/articles\/wp-json\/wp\/v2\/media\/11176"}],"wp:attachment":[{"href":"https:\/\/credevo.com\/articles\/wp-json\/wp\/v2\/media?parent=11173"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/credevo.com\/articles\/wp-json\/wp\/v2\/categories?post=11173"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/credevo.com\/articles\/wp-json\/wp\/v2\/tags?post=11173"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}