{"id":50609,"date":"2022-11-09T16:35:27","date_gmt":"2022-11-09T11:05:27","guid":{"rendered":"https:\/\/corpbiz.io\/learning\/?p=50609"},"modified":"2025-08-13T10:32:52","modified_gmt":"2025-08-13T05:02:52","slug":"cdsco-registration-for-nephrology-and-renal-care-medical-devices","status":"publish","type":"post","link":"https:\/\/corpbiz.io\/learning\/cdsco-registration-for-nephrology-and-renal-care-medical-devices\/","title":{"rendered":"CDSCO Registration for Nephrology and Renal Care Medical Devices \u2013 An Overview"},"content":{"rendered":"\n<p>There is an assortment of\nmedical devices used in the diagnosis and treatment of kidney-related diseases.\nThe devices that fall under the class A and B risk categories will now come\nunder the ambit of CDSCO. The registration of such devices has been made\ncompulsory by the authority, which will become effective from 1st Oct\n2022.&nbsp; It&#8217;s worth noting that only\nmanufacturers and importers of such devices fall under the CDCSCO licensing\nscheme. In this write-up, we will learn about the <strong><a class=\"text-primary\" href=\"https:\/\/corpbiz.io\/cdsco-registration\" title=\"CDSCO registration Online\">CDSCO Registration<\/a><\/strong> for Nephrology and Renal Care medical devices in\ndetail. <\/p>\n\n\n\n<div id=\"ez-toc-container\" class=\"ez-toc-v2_0_82_2 counter-hierarchy ez-toc-counter ez-toc-grey ez-toc-container-direction\">\n<div class=\"ez-toc-title-container\">\n<p class=\"ez-toc-title ez-toc-toggle\" style=\"cursor:pointer\">Page Contents<\/p>\n<span class=\"ez-toc-title-toggle\"><a href=\"#\" class=\"ez-toc-pull-right ez-toc-btn ez-toc-btn-xs ez-toc-btn-default ez-toc-toggle\" aria-label=\"Toggle Table of Content\"><span class=\"ez-toc-js-icon-con\"><span class=\"\"><span class=\"eztoc-hide\" style=\"display:none;\">Toggle<\/span><span class=\"ez-toc-icon-toggle-span\"><svg style=\"fill: #999;color:#999\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" class=\"list-377408\" width=\"20px\" height=\"20px\" viewBox=\"0 0 24 24\" fill=\"none\"><path d=\"M6 6H4v2h2V6zm14 0H8v2h12V6zM4 11h2v2H4v-2zm16 0H8v2h12v-2zM4 16h2v2H4v-2zm16 0H8v2h12v-2z\" fill=\"currentColor\"><\/path><\/svg><svg style=\"fill: #999;color:#999\" class=\"arrow-unsorted-368013\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" width=\"10px\" height=\"10px\" viewBox=\"0 0 24 24\" version=\"1.2\" baseProfile=\"tiny\"><path d=\"M18.2 9.3l-6.2-6.3-6.2 6.3c-.2.2-.3.4-.3.7s.1.5.3.7c.2.2.4.3.7.3h11c.3 0 .5-.1.7-.3.2-.2.3-.5.3-.7s-.1-.5-.3-.7zM5.8 14.7l6.2 6.3 6.2-6.3c.2-.2.3-.5.3-.7s-.1-.5-.3-.7c-.2-.2-.4-.3-.7-.3h-11c-.3 0-.5.1-.7.3-.2.2-.3.5-.3.7s.1.5.3.7z\"\/><\/svg><\/span><\/span><\/span><\/a><\/span><\/div>\n<nav><ul class='ez-toc-list ez-toc-list-level-1 eztoc-toggle-hide-by-default' ><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-1\" href=\"https:\/\/corpbiz.io\/learning\/cdsco-registration-for-nephrology-and-renal-care-medical-devices\/#What_is_Nephrology_and_Renal_care\" >What is Nephrology and Renal care?<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-2\" href=\"https:\/\/corpbiz.io\/learning\/cdsco-registration-for-nephrology-and-renal-care-medical-devices\/#List_of_Notified_Medical_devices_relating_to_Nephrology_and_Renal_Care\" >List of Notified Medical devices relating to Nephrology and Renal Care<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-3\" href=\"https:\/\/corpbiz.io\/learning\/cdsco-registration-for-nephrology-and-renal-care-medical-devices\/#What_is_the_Role_of_CDSCO\" >What is the Role of CDSCO?<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-4\" href=\"https:\/\/corpbiz.io\/learning\/cdsco-registration-for-nephrology-and-renal-care-medical-devices\/#Legal_Definition_of_the_Medical_Devices\" >Legal Definition of the Medical Devices<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-5\" href=\"https:\/\/corpbiz.io\/learning\/cdsco-registration-for-nephrology-and-renal-care-medical-devices\/#Categorization_of_Medical_Devices_in_India\" >Categorization of Medical Devices in India<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-6\" href=\"https:\/\/corpbiz.io\/learning\/cdsco-registration-for-nephrology-and-renal-care-medical-devices\/#Eligibility_norms_CDSCO_Registration_for_Nephrology_and_Renal_Care_Medical_Devices\" >Eligibility norms CDSCO Registration for Nephrology and Renal Care Medical Devices<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-7\" href=\"https:\/\/corpbiz.io\/learning\/cdsco-registration-for-nephrology-and-renal-care-medical-devices\/#Documentations_to_be_uploaded_by_Applicant_for_CDSCO_Registration_for_Nephrology_and_Renal_Care\" >Documentations to be uploaded by Applicant for CDSCO Registration for Nephrology and Renal Care<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-8\" href=\"https:\/\/corpbiz.io\/learning\/cdsco-registration-for-nephrology-and-renal-care-medical-devices\/#Process_and_Fee_relating_to_CDSCO_Registration_for_Nephrology_and_Renal_Care_Medical_Devices\" >Process and Fee relating to CDSCO Registration for Nephrology and Renal Care Medical Devices<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-9\" href=\"https:\/\/corpbiz.io\/learning\/cdsco-registration-for-nephrology-and-renal-care-medical-devices\/#Key_points_to_ponder_regarding_CDSCO_Registration_for_Nephrology_and_Renal_Care\" >Key points to ponder regarding CDSCO Registration for Nephrology and Renal Care<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-10\" href=\"https:\/\/corpbiz.io\/learning\/cdsco-registration-for-nephrology-and-renal-care-medical-devices\/#Conclusion\" >Conclusion<\/a><\/li><\/ul><\/nav><\/div>\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"What_is_Nephrology_and_Renal_care\"><\/span>What is Nephrology and Renal care? <span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>Nephrology is a medical\nfield that deals with the study of kidneys and their diseases. The nephrologist\ndeals with the treatment and diagnosis of kidney-related conditions. The\nkidneys ensure the optimal presence of fluid and electrolytes in the body.\nRenal clearance test measures the kidney\u2019s capacity to segregate compounds from\nthe human blood. Further, the creatinine clearance test gauges the glomerular\nfiltration rate. Weakened kidney performance can lead to waste build-up within\nthe blood, causing various diseases in the human body. <\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"List_of_Notified_Medical_devices_relating_to_Nephrology_and_Renal_Care\"><\/span>List of Notified Medical devices relating to Nephrology and Renal Care<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>The category concerning Nephrology and renal care comprises a total of 15 medical devices categorized on a risk-wise basis and intended use. However, Class A and B devices will only come under the ambit of CDSCO registration. Here is the list of devices requiring CDSCO approval:<\/p>\n\n\n\n<ol>\n<li>Urinary Stone Retrieval\nbasket <\/li>\n\n\n\n<li>Crimp for plier,\nHemodialysis<\/li>\n\n\n\n<li>Chair, Haemodialysism\nelectrically powered\/manual<\/li>\n\n\n\n<li>Dialyser connector <\/li>\n\n\n\n<li>Laser Lithotripsy\nfiber\/suction guide<\/li>\n\n\n\n<li>Flexible fiber optic\nnephoscopy<\/li>\n\n\n\n<li>Hemodialysis blood\ntubing\/Extracorporeal systems <\/li>\n\n\n\n<li>The peritoneal dialysis\ncatheter guidewire<\/li>\n\n\n\n<li>Rigid nephroscope<\/li>\n\n\n\n<li>Peritoneal dialysis ultraviolet irradiation unit<\/li>\n\n\n\n<li>Stunts thrombus suction set<\/li>\n\n\n\n<li>Rigid nephroscope<\/li>\n\n\n\n<li>Portable continuous peritoneal perfusate thermal conditioner<\/li>\n\n\n\n<li>Extracorporeal circuit waste bag<\/li>\n\n\n\n<li>Citric acid hemodialysis system cleaning cartridge<\/li>\n<\/ol>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"What_is_the_Role_of_CDSCO\"><\/span>What is the Role of CDSCO? <span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>CDSCO stands for Central\nDrug Standard Control Organization is a government-backed legislative body that\nregulates the manufacturing and selling of drugs and medical devices in India.\nThe authority underpins various norms and guidelines to ensure the production\nand trading of safer pharma products.&nbsp;\nCDSCO devises guidelines in accordance with the <strong>Drugs and Cosmetic Act 1940<\/strong><sup><a class=\"text-primary\" href=\"https:\/\/en.wikipedia.org\/wiki\/Drugs_and_Cosmetics_Act,_1940\"><strong>[1]<\/strong><\/a><\/sup>.\nPresently, 37 categories of medical devices fall under the CDSCO\u2019s licensing\nscheme. The Drugs and Cosmetic Act 1940 governs the entire supply chain of\nthese medical devices and it even applies to importable goods. <\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Legal_Definition_of_the_Medical_Devices\"><\/span>Legal Definition of the Medical Devices <span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>Medical Devices Amendment\nRules 2022 defines medical devices as devices utilized in typical medical\npractice such as impact appliances, medical apparatus, and instruments. As per\nthe said rules, a device is qualified to be called a medical device if it\nserves the following purpose.<\/p>\n\n\n\n<ul>\n<li>Help in diagnosing or\ntreating the body\u2019s disorder, disease, or injury. <\/li>\n\n\n\n<li>Help in supporting and\nsustaining life<\/li>\n\n\n\n<li>Support in the finding of\nan anatomy <\/li>\n<\/ul>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Categorization_of_Medical_Devices_in_India\"><\/span>Categorization of Medical Devices in India <span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>The New Medical Rules,\n2015 has categorized medical devices under four classes based on their risk\nlevel and usability.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\"><em>Class A: <\/em><\/h3>\n\n\n\n<p>Devices under this class\nadhere to low-risk. Some examples include tongues depressure, thermometer, and\nso on.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\"><em>Class B: <\/em><\/h3>\n\n\n\n<p>Devices under this class\nhave low moderate risk. Products like suction equipment and hypodermic needles\nfall under this class.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\"><em>Class C<\/em>:<\/h3>\n\n\n\n<p>Devices of the Class C\ncategory have moderate-high risk. A lung ventilator is a medical device that\nbelongs to this category.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\"><em>Class D:<\/em><\/h3>\n\n\n\n<p>Medical Devices that fall\nunder this category are considered to be highly risky. Some examples include\nimplant devices and heart valves. <\/p>\n\n\n\n<p>The permission of\nmanufacturing Class A and B devices is granted by the State Licensing\nAuthority. Similarly, for manufacturing Class C and D devices, one has to\nobtain approval\/certification from the Central Licensing Authority.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Eligibility_norms_CDSCO_Registration_for_Nephrology_and_Renal_Care_Medical_Devices\"><\/span>Eligibility norms CDSCO Registration for Nephrology and Renal Care Medical Devices<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>Drug and Cosmetic Act 1940 and Rules 1945 entail the provisions concerning the manufacturing, import, sale, and distribution of medical devices. Thus, any individual\/company with a <strong><a href=\"https:\/\/corpbiz.io\/wholesale-drug-license\">wholesale drug license<\/a><\/strong> or production license granted under these Acts can file an application for licensing and import of medical devices into India. <\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Documentations_to_be_uploaded_by_Applicant_for_CDSCO_Registration_for_Nephrology_and_Renal_Care\"><\/span>Documentations to be uploaded by Applicant for CDSCO Registration for Nephrology and Renal Care<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>Following is the list of documents required\nfor CDSCO Registration for Nephrology and Renal Care:<\/p>\n\n\n\n<ul>\n<li>Application Form<\/li>\n\n\n\n<li>Quality Assurance\nCertificate <\/li>\n\n\n\n<li>ISO 13485 certificate <\/li>\n\n\n\n<li>Undertaking confirming\nthat the provided details are legitimate. <\/li>\n\n\n\n<li>CE design certificate <\/li>\n\n\n\n<li>Either a Certificate from\nthe overseas government or a Free sale certificate<\/li>\n\n\n\n<li>Marketability certificate\nfrom GHTF<\/li>\n\n\n\n<li>Device master file <\/li>\n\n\n\n<li>Plant master report <\/li>\n<\/ul>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Process_and_Fee_relating_to_CDSCO_Registration_for_Nephrology_and_Renal_Care_Medical_Devices\"><\/span>Process and Fee relating to CDSCO Registration for Nephrology and Renal Care Medical Devices<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>The followings are the types of <strong><a href=\"https:\/\/corpbiz.io\/medical-device-registration\" title=\"Medical device registration in India\">medical device registration<\/a><\/strong>; <\/p>\n\n\n\n<ul>\n<li>Registration\/Importation\nof any medical device in existence;<\/li>\n\n\n\n<li>Registration\/Importation\nof any medical device that is new in the market<\/li>\n<\/ul>\n\n\n\n<p><strong><em>The process for\nregistering medical devices in India is as follows; <\/em><\/strong><\/p>\n\n\n\n<h3 class=\"wp-block-heading\"><em>Step 1: Find whether your product falls under the notified list or not<\/em><\/h3>\n\n\n\n<p>The CDSCO has devised a list of notified medical devices based on risk-level categorization as mentioned above. Products under Class C and D require CDSCO\u2019s approval in the form of registration as per the Drug and Cosmetics Act 1940 and Medical Devices rules 2017. However, in the case of non-listed devices or new equipment, the manufacturer\/importer may need to <strong><a href=\"https:\/\/corpbiz.io\/noc-from-assistant-drug-controller\" title=\"NOC Apply Online\">apply for an NOC<\/a><\/strong>. <\/p>\n\n\n\n<p>For instance, products\nlike condoms, surgical apparel, Tubal Rings, and Intra-Uterine devices do not\nrequire CDSCO\u2019s approval. Similarly, devices falling under the moderate to\nhigh-risk categories such as Needles, cochlear implants, heart valves,\ncatheters, and spinal needles fall under the compulsory registration scheme. <\/p>\n\n\n\n<h3 class=\"wp-block-heading\"><em>Step 2: Appoint an AIR i.e Authorized Indian Representative (in case of an overseas company) <\/em><\/h3>\n\n\n\n<p>Unlike Indian entities, overseas firms cannot approach directly CDCSO to apply for a license. For this purpose, they need a legal mediator (technically known as an Authorized Indian Representative) who will address the registration legalities on their behalf. Such a representative must have a wholesale <strong><a href=\"https:\/\/corpbiz.io\/drug-license\">drug license<\/a><\/strong> in forms 20B &amp; 21B.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\"><em>Step 3: Fill out the registration application form<\/em><\/h3>\n\n\n\n<p>In this crucial step, the\napplicant (manufacturer\/importer\/AIR) must visit the CDSCO portal for online\napplication filing for registration. While applying online, the applicant should\nupload all the mandatory documentation in the requested format. Once done, head\nto the payment gateway for fee submission. The successful payment will lead to\nthe completion of the online filing process.&nbsp;\nThe table below reflects the different forms required to serve specific\npurposes. <\/p>\n\n\n\n<table class=\"table table-bordered\"><tbody><tr><td>\n  <strong><em>Applicant <\/em><\/strong>\n  <\/td><td>\n  <strong><em>Class of\n  Medical Devices <\/em><\/strong>\n  <\/td><td>\n  <strong><em>Application\n  Form <\/em><\/strong>\n  <\/td><td>\n  <strong><em>License\n  Form<\/em><\/strong>\n  <\/td><\/tr><tr><td>\n  Manufacturer \n  <\/td><td>\n  A, B\n  <\/td><td>\n  MD-3\n  <\/td><td>\n  MD-5\n  <\/td><\/tr><tr><td>\n  Importer \n  <\/td><td>\n  A, B, C, D\n  <\/td><td>\n  MD-14\n  <\/td><td>\n  MD-15\n  <\/td><\/tr><tr><td>\n  Manufacturer\n  \n  <\/td><td>\n  C, D\n  <\/td><td>\n  MD-7\n  <\/td><td>\n  MD-9\n  <\/td><\/tr><tr><td>\n  Manufacturer\n  (Loan License)\n  <\/td><td>\n  A, B\n  <\/td><td>\n  MD-4\n  <\/td><td>\n  MD-6\n  <\/td><\/tr><tr><td>\n  Manufacturer\n  (Loan License)\n  <\/td><td>\n  C, D\n  <\/td><td>\n  MD-8\n  <\/td><td>\n  MD-10\n  <\/td><\/tr><\/tbody><\/table>\n\n\n\n<h3 class=\"wp-block-heading\"><em>Step 4: Secure license in the prescribed form <\/em><\/h3>\n\n\n\n<p>Post application\nsubmission, the concerned authority may send an inquiry letter enclosing the\nlist of questions to the applicant. The recipient must reply to all the questions\nwithin the prescribed timeframe. In some cases, the recipient may have to\nundergo a technical presentation on the authority\u2019s directions. After\nfulfilling all such requirements, the authority will accord the license in the\nstandard form. <\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Key_points_to_ponder_regarding_CDSCO_Registration_for_Nephrology_and_Renal_Care\"><\/span>Key points to ponder regarding CDSCO Registration for Nephrology and Renal Care<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>Following are some vital points regarding\nCDSCO Registration for Nephrology and Renal Care Medical Devices:<\/p>\n\n\n\n<ul>\n<li>DGCI usually grants the\nlicense within 6-9 months in case no technical presentation is demanded.\nConversely, if a technical presentation is required, the authority will take\n3-5 months for stamping their approval.<\/li>\n\n\n\n<li>The license granted to the\nmanufacturer\/importer shall remain valid for 3 years. <\/li>\n\n\n\n<li>Any changes made to the\ncurrent premises or production unit should be intimated to the Authority in\nwriting. The same rule applies to the case of unit relocation.<\/li>\n\n\n\n<li>In the above scenarios,\nthe registration validity comes down to three months. This three months\u2019\ntimeline must be used by the applicant to address fresh certificated\nformalities. <\/li>\n<\/ul>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Conclusion\"><\/span>Conclusion <span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>It is evident from the above that CDSCO\u2019s approval is a must for applicants seeking to engage with the manufacturing or <strong><a href=\"https:\/\/corpbiz.io\/cdsco-drugs-import-license\" title=\"Drugs Import in India\">import of drugs<\/a><\/strong> and medical devices. CDSCO Registration for Nephrology and Renal Care medical devices is the only way to start the business legally.&nbsp; <\/p>\n\n\n\n<p class=\"text-left\"><b>Read Our Article<\/b>:<mark style=\"background: #fffd03 !important;\"><a href=\"https:\/\/corpbiz.io\/learning\/registration-process-for-medical-devices-in-india\/\">A Step by Step guide for Registration Process for Medical Devices in India<\/a><\/mark><\/p>\n","protected":false},"excerpt":{"rendered":"<p>There is an assortment of medical devices used in the diagnosis and treatment of kidney-related diseases. The devices that fall under the class A and B risk categories will now come under the ambit of CDSCO. The registration of such devices has been made compulsory by the authority, which will become effective from 1st Oct [&hellip;]<\/p>\n","protected":false},"author":22,"featured_media":50610,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[2358],"tags":[2845],"acf":{"service_id":"508"},"authorName":"Pankaj Tyagi","authorImageUrl":"https:\/\/corpbiz.io\/learning\/wp-content\/uploads\/2022\/01\/MicrosoftTeams-image-42.jpg","authorDescription":"Pankaj has a diverse experience of writing research papers, blog, and articles during his college time. Earlier, he was working as a tax consultant in a financial firm, but his interest in writing drives him to pursue a career in the writing field.","postViews":2889,"readingTime":5,"_links":{"self":[{"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/posts\/50609"}],"collection":[{"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/users\/22"}],"replies":[{"embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/comments?post=50609"}],"version-history":[{"count":5,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/posts\/50609\/revisions"}],"predecessor-version":[{"id":69817,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/posts\/50609\/revisions\/69817"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/media\/50610"}],"wp:attachment":[{"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/media?parent=50609"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/categories?post=50609"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/tags?post=50609"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}