{"id":49550,"date":"2022-10-01T17:36:00","date_gmt":"2022-10-01T12:06:00","guid":{"rendered":"https:\/\/corpbiz.io\/learning\/?p=49550"},"modified":"2022-10-01T17:36:02","modified_gmt":"2022-10-01T12:06:02","slug":"cdsco-medical-device-registration-for-pacemaker","status":"publish","type":"post","link":"https:\/\/corpbiz.io\/learning\/cdsco-medical-device-registration-for-pacemaker\/","title":{"rendered":"CDSCO Medical Device Registration for Pacemaker: Complete Guide"},"content":{"rendered":"\n<p>The DCGI issued a notice on July 26th 2021, stating the classification of medical devices pertaining to cardiovascular devices, per the provisions of medical device rules 2017. According to the classification, 36 non-notified devices be regulated as medical devices for the treatment of cardiovascular problems under the Medical Device Rules, 2017. The regulatory authorities have also mandated CDSCO <a href=\"https:\/\/corpbiz.io\/medical-device-registration\"><strong>Medical Device Registration<\/strong><\/a> for Pacemakers as a part of cardiovascular medical devices. <\/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-medical-device-registration-for-pacemaker\/#Overview_of_CDSCO_Regulation_on_Medical_Devices\" >Overview of CDSCO Regulation on Medical Devices<\/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-medical-device-registration-for-pacemaker\/#CDSCO_Non-Notified_Medical_Device_Classification\" >CDSCO Non-Notified Medical Device Classification<\/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-medical-device-registration-for-pacemaker\/#Classification_of_Cardiovascular_Medical_Devices\" >Classification of Cardiovascular Medical Devices<\/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-medical-device-registration-for-pacemaker\/#Documents_required_for_CDSCO_Medical_Device_Registration_for_Pacemaker\" >Documents required for CDSCO Medical Device Registration for Pacemaker<\/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-medical-device-registration-for-pacemaker\/#Procedure_for_CDSCO_Medical_Device_Registration_for_Pacemaker\" >Procedure for CDSCO Medical Device Registration for Pacemaker<\/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-medical-device-registration-for-pacemaker\/#Conclusion\" >Conclusion<\/a><\/li><\/ul><\/nav><\/div>\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Overview_of_CDSCO_Regulation_on_Medical_Devices\"><\/span><strong>Overview of CDSCO Regulation on Medical Devices <\/strong><span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>Central Drug\nStandard Control Organization, or CDSCO, is the National Regulatory Authority\nof India and is responsible for regulating Medical Devices, IVDs and Drugs in\nIndia. It works under the Ministry of Health and Family Welfare, which the\nDirectorate General of Health Services regulates under the Indian Government.\nCDSCO is also governed by the Drugs and Cosmetics act and is known as the\nCentral Drug Authority of India.<\/p>\n\n\n\n<p>A Medical Device may be any instrument, tool,\u00a0 implement, machine, apparatus, appliance, implant, and reagent for in vitro use, material, software, or any other related article,&#8221; according to the definition provided by the <strong>FDA<\/strong><sup><a href=\"https:\/\/en.wikipedia.org\/wiki\/Food_and_Drug_Administration\"><strong>[1]<\/strong><\/a><\/sup>.<\/p>\n\n\n\n<p><strong><em>A\nmedical device can be one of two categories:<\/em><\/strong><\/p>\n\n\n\n<ul><li>Notified medical device<\/li><li>Not Notified medical device<\/li><\/ul>\n\n\n\n<p>The Medical\nDevice Rules, 2017, were brought into effect on January 1st 2018, by the CDSCO.\nThe Central Drug Standard Control Organization (CDSCO) divided medical devices\nbetween India into four different classes- Class A, B, C and D. Under this\nclassification, medical devices are categorized based on the risks involved.\nThe different classes of devices involve different licensing procedures and\nrequirements.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"CDSCO_Non-Notified_Medical_Device_Classification\"><\/span><strong>CDSCO Non-Notified Medical Device Classification<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>Earlier, only 37 medical devices were regulated by\nCDSCO. But in a recent notification, there has been a list of non-notified\ndevices that falls under the definition of Medical Devices in India. The\nMinistry of Health and Family Welfare has recently amended the Medical Device\nRules, 2017. According to a notice issued by CDSCO on February 11th 2020, it\nwas notified that all medical devices are to be voluntarily registered with\nCDSCO before the deadline. After the deadline, registration will be made\nmandatory for those devices. The deadline for voluntarily registering medical\ndevices of Class A and B is October 1st 2022, and for Medical devices of class\nC and D is October 1st 2023.&nbsp; <\/p>\n\n\n\n<p>CDSCO issued another notice on September 3rd 2020,\nwhich included 24 non-notified medical devices for registration. CDSCO Medical\nDevice Registration for Pacemaker is classified under cardiovascular medical\ndevice, which is a part of the list. The classification of 24 newly listed non-\nnotified devices are- <\/p>\n\n\n\n<table class=\"table table-bordered\">\n<tbody>\n<tr>\n<td width=\"66\">\n<p><strong>S.L. No.<\/strong><\/p>\n<\/td>\n<td width=\"283\">\n<p><strong>Categories of medical device<\/strong><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td width=\"66\">\n<p>1<\/p>\n<\/td>\n<td width=\"283\">\n<p>Anaesthesiology&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<\/p>\n<\/td>\n<\/tr>\n<tr>\n<td width=\"66\">\n<p>2<\/p>\n<\/td>\n<td width=\"283\">\n<p>Pain Management&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<\/p>\n<\/td>\n<\/tr>\n<tr>\n<td width=\"66\">\n<p>3<\/p>\n<\/td>\n<td width=\"283\">\n<p>Cardiovascular&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<\/p>\n<\/td>\n<\/tr>\n<tr>\n<td width=\"66\">\n<p>4<\/p>\n<\/td>\n<td width=\"283\">\n<p>Dental&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<\/p>\n<\/td>\n<\/tr>\n<tr>\n<td width=\"66\">\n<p>5<\/p>\n<\/td>\n<td width=\"283\">\n<p>Ear, Nose, Throat (ENT)&nbsp;&nbsp;&nbsp;&nbsp;<\/p>\n<\/td>\n<\/tr>\n<tr>\n<td width=\"66\">\n<p>6<\/p>\n<\/td>\n<td width=\"283\">\n<p>Gastroenterological&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<\/p>\n<\/td>\n<\/tr>\n<tr>\n<td width=\"66\">\n<p>7<\/p>\n<\/td>\n<td width=\"283\">\n<p>Urological&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<\/p>\n<\/td>\n<\/tr>\n<tr>\n<td width=\"66\">\n<p>8<\/p>\n<\/td>\n<td width=\"283\">\n<p>General Hospital&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<\/p>\n<\/td>\n<\/tr>\n<tr>\n<td width=\"66\">\n<p>9<\/p>\n<\/td>\n<td width=\"283\">\n<p>Operation Theater (O.T.)&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<\/p>\n<\/td>\n<\/tr>\n<tr>\n<td width=\"66\">\n<p>10<\/p>\n<\/td>\n<td width=\"283\">\n<p>Respiratory&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Classification_of_Cardiovascular_Medical_Devices\"><\/span><strong>Classification of Cardiovascular Medical Devices <\/strong><span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>Cardiovascular medical devices are classified into\nvarious classes according to the intended use and risk classification. The CDSCO Medical Device Registration for Pacemaker has\nbeen made mandatory by CDSCO as different devices pacemakers have also been included\nin the classification, listed as follows- <\/p>\n\n\n\n<table class=\"table table-bordered\"><tbody><tr><td>\n  Sr.No. <em><\/em>\n  <\/td><td>\n  Medical Device Name <em><\/em>\n  <\/td><td>\n  Risk Class <em><\/em>\n  <\/td><\/tr><tr><td>\n  1 <em><\/em>\n  <\/td><td>\n  Arrhythmia Detector And Alarm (Including St-Segment\n  Measurement And Alarm) \n  <\/td><td>\n  C \n  <\/td><\/tr><tr><td>\n  2 <em><\/em>\n  <\/td><td>\n  Cardiac monitor (including cardio tachometer and rate alarm\n  <\/td><td>\n  B \n  <\/td><\/tr><tr><td>\n  3 <em><\/em>\n  <\/td><td>\n  Apexcardiograph (vibrocardiograph)&nbsp; \n  <\/td><td>\n  B&nbsp; \n  <\/td><\/tr><tr><td>\n  4 <em><\/em>\n  <\/td><td>\n  Echocardiography \n  <\/td><td>\n  B \n  <\/td><\/tr><tr><td>\n  5 <em><\/em>\n  <\/td><td>\n  Electrocardiograph \n  <\/td><td>\n  B \n  <\/td><\/tr><tr><td>\n  6 <em><\/em>\n  <\/td><td>\n  Electrocardiograph electrode\n  <\/td><td>\n  B \n  <\/td><\/tr><tr><td>\n  7 <em><\/em>\n  <\/td><td>\n  Vascular clip \n  <\/td><td>\n  B \n  <\/td><\/tr><tr><td>\n  8 <em><\/em>\n  <\/td><td>\n  Vena cava clip \n  <\/td><td>\n  B \n  <\/td><\/tr><tr><td>\n  9 <em><\/em>\n  <\/td><td>\n  Intra-aortic balloon \n  <\/td><td>\n  C \n  <\/td><\/tr><tr><td>\n  10<em><\/em>\n  <\/td><td>\n  &nbsp;Intra-aortic balloon control\n  system (balloon pump) \n  <\/td><td>\n  B\n  <\/td><\/tr><tr><td>\n  11 <em><\/em>\n  <\/td><td>\n  Ventricular bypass (assist) device \n  <\/td><td>\n  D \n  <\/td><\/tr><tr><td>\n  12 <em><\/em>\n  <\/td><td>\n  Pacing system analyzer \n  <\/td><td>\n  C \n  <\/td><\/tr><tr><td>\n  13<em><\/em>\n  <\/td><td>\n  &nbsp;The implantable\n  pacemaker pulse generator \n  <\/td><td>\n  D \n  <\/td><\/tr><tr><td>\n  14 <em><\/em>\n  <\/td><td>\n  Pacemaker lead adaptor \n  <\/td><td>\n  C \n  <\/td><\/tr><tr><td>\n  15 <em><\/em>\n  <\/td><td>\n  Pacemaker generator function analyzer \n  <\/td><td>\n  C \n  <\/td><\/tr><tr><td>\n  16 <em><\/em>\n  <\/td><td>\n  Cardiovascular permanent or temporary pacemaker electrode \n  <\/td><td>\n  C \n  <\/td><\/tr><tr><td>\n  17 <em><\/em>\n  <\/td><td>\n  Pacemaker test magnet \n  <\/td><td>\n  A \n  <\/td><\/tr><tr><td>\n  18 <em><\/em>\n  <\/td><td>\n  Pacemaker programmers \n  <\/td><td>\n  C \n  <\/td><\/tr><tr><td>\n  19<em><\/em>\n  <\/td><td>\n  Pacemaker repair or replacement material \n  <\/td><td>\n  D \n  <\/td><\/tr><tr><td>\n  20 <em><\/em>\n  <\/td><td>\n  Annuloplasty ring \n  <\/td><td>\n  C \n  <\/td><\/tr><tr><td>\n  21 <em><\/em>\n  <\/td><td>\n  Carotid sinus nerve stimulator \n  <\/td><td>\n  D&nbsp; \n  <\/td><\/tr><tr><td>\n  22 <em><\/em>\n  <\/td><td>\n  Replacement heart valve \n  <\/td><td>\n  D \n  <\/td><\/tr><tr><td>\n  23 <em><\/em>\n  <\/td><td>\n  Endomyocardial biopsy device \n  <\/td><td>\n  D \n  <\/td><\/tr><tr><td>\n  24 <em><\/em>\n  <\/td><td>\n  Extracorporeal circuit and accessories for long-term\n  respiratory\/cardiopulmonary failure \n  <\/td><td>\n  C \n  <\/td><\/tr><tr><td>\n  25 <em><\/em>\n  <\/td><td>\n  Cardiopulmonary bypass bubble detector \n  <\/td><td>\n  B \n  <\/td><\/tr><tr><td>\n  26 <em><\/em>\n  <\/td><td>\n  Cardiopulmonary bypass vascular catheter, cannula, or tubing \n  <\/td><td>\n  B \n  <\/td><\/tr><tr><td>\n  27 <em><\/em>\n  <\/td><td>\n  Cardiopulmonary bypass heart-lung machine console\n  <\/td><td>\n  B \n  <\/td><\/tr><tr><td>\n  28 <em><\/em>\n  <\/td><td>\n  Cardiopulmonary bypass defoamer \n  <\/td><td>\n  C \n  <\/td><\/tr><tr><td>\n  29 <em><\/em>\n  <\/td><td>\n  Cardiopulmonary bypass heat exchanger \n  <\/td><td>\n  B \n  <\/td><\/tr><tr><td>\n  30 <em><\/em>\n  <\/td><td>\n  Cardiopulmonary bypass temperature controller \n  <\/td><td>\n  B \n  <\/td><\/tr><tr><td>\n  31 <em><\/em>\n  <\/td><td>\n  Cardiopulmonary bypass arterial line blood filter \n  <\/td><td>\n  C \n  <\/td><\/tr><tr><td>\n  32 <em><\/em>\n  <\/td><td>\n  Cardiopulmonary bypass cardiotomy suction line blood \n  <\/td><td>\n  B \n  <\/td><\/tr><tr><td>\n  33 <em><\/em>\n  <\/td><td>\n  Cardiopulmonary bypass pulsatile flow generator \n  <\/td><td>\n  D \n  <\/td><\/tr><tr><td>\n  34 <em><\/em>\n  <\/td><td>\n  Intraluminal artery stripper \n  <\/td><td>\n  B \n  <\/td><\/tr><tr><td>\n  35<em><\/em>\n  <\/td><td>\n  External cardiac compressor \n  <\/td><td>\n  C \n  <\/td><\/tr><tr><td>\n  36 <em><\/em>\n  <\/td><td>\n  External transcutaneous cardiac pacemaker \n  <\/td><td>\n  C \n  <\/td><\/tr><\/tbody><\/table>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Documents_required_for_CDSCO_Medical_Device_Registration_for_Pacemaker\"><\/span><strong>Documents required for CDSCO Medical Device Registration for Pacemaker<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>The following is\na list of the requirements for CDSCO Medical Device Registration for Pacemakers<\/p>\n\n\n\n<ul><li>Application form for registration <\/li><li>Challan TR6<\/li><li>ISO 13485<\/li><li>Power of Attorney<\/li><li>An Undertaking stating that only accurate\ninformation is provided<\/li><li>Certificate of quality assurance<\/li><li>C.E. Design accreditation<\/li><li>Declaration of conformity<\/li><li>Schedule D(I)<\/li><li>Master Plant File<\/li><li>Device master file <\/li><li>Free sale certificate<\/li><\/ul>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Procedure_for_CDSCO_Medical_Device_Registration_for_Pacemaker\"><\/span><strong>Procedure for CDSCO Medical Device Registration for Pacemaker<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>The process for CDSCO\nMedical Device Registration for Pacemakers in India is listed below. &#8211;<\/p>\n\n\n\n<ul><li><strong>Identify whether the medical devices need to be registered:<\/strong> To determine whether a medical device has been notified or not, the applicant must first check the Medical Devices and IVDs list. Before being marketed in India, all non- notified medical devices must obtain voluntary registration before the deadline. <\/li><li><strong>Indian Authorized Agent Appointment:<\/strong> In the case where the manufacturer is not Indian, an IAA, or Indian Authorized Agent, is appointed. The IAA represents the manufacturer in court and carries out all of their official business in India.<\/li><li><strong>Documentation procedure:<\/strong> To obtain a registration license, all required paperwork must be submitted to the appropriate authorities.<\/li><li><strong>Obtaining Registration and License:<\/strong> The manufacturer receives the registration license after submitting all required paperwork to the appropriate authorities.<\/li><\/ul>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Conclusion\"><\/span><strong>Conclusion<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>Central Drug Standard Control Organization has issued a new risk-based Classification for Cardiovascular Medical Devices in India to comply with the latest medical equipment rules in India.CDSCO Medical Device Registration for Pacemakers is a part of the classification based on the cardiovascular medical device. The notice was issued on July 26th 2021, stating that Cardiovascular Medical Devices are classified as Non-Notified Medical Devices by CDSCO. The classification includes 24 medical devices. It is always advisable to connect with an experienced professional for CDSCO Registration for Medical Device Registration for Pacemaker to save time and money wasted on any failure. <\/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\/cdsco-registration-for-dermatology-and-plastic-surgery-medical-devices\/\">CDSCO Registration for Dermatology and Plastic Surgery Medical Devices<\/a><\/mark><\/p>\n","protected":false},"excerpt":{"rendered":"<p>The DCGI issued a notice on July 26th 2021, stating the classification of medical devices pertaining to cardiovascular devices, per the provisions of medical device rules 2017. According to the classification, 36 non-notified devices be regulated as medical devices for the treatment of cardiovascular problems under the Medical Device Rules, 2017. The regulatory authorities have [&hellip;]<\/p>\n","protected":false},"author":45,"featured_media":49552,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[2358],"tags":[2759],"acf":{"service_id":"508"},"authorName":"Snehita Shukla","authorImageUrl":"https:\/\/corpbiz.io\/learning\/wp-content\/uploads\/2022\/07\/MicrosoftTeams-image-84.jpg","authorDescription":"Snehita has her qualifications in B.Com LLB and LLM, and holds a specialization in Corporate &amp; Financial Laws and Policy. She is hardworking, dedicated and sincere. She has a great command in english and has great problem solving, critical thinking  and writing skills which makes her stand out of the crowd. She has a keen interest in legal research work and content writing, she also has a hold in legal research methodology. She loves to take challenges and to explore new topics to research on. She aims to improve her knowledge and skills through her experience.","postViews":3411,"readingTime":4,"_links":{"self":[{"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/posts\/49550"}],"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\/45"}],"replies":[{"embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/comments?post=49550"}],"version-history":[{"count":17,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/posts\/49550\/revisions"}],"predecessor-version":[{"id":49570,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/posts\/49550\/revisions\/49570"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/media\/49552"}],"wp:attachment":[{"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/media?parent=49550"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/categories?post=49550"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/tags?post=49550"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}