{"id":9005,"date":"2020-05-20T15:18:47","date_gmt":"2020-05-20T09:48:47","guid":{"rendered":"https:\/\/corpbiz.io\/learning\/?p=9005"},"modified":"2020-12-30T12:38:42","modified_gmt":"2020-12-30T07:08:42","slug":"how-to-get-a-manufacturing-license-of-drugs-in-india","status":"publish","type":"post","link":"https:\/\/corpbiz.io\/learning\/how-to-get-a-manufacturing-license-of-drugs-in-india\/","title":{"rendered":"How to get a Manufacturing License of Drugs in India?"},"content":{"rendered":"\n<p class=\"has-drop-cap\">The company\/distributor\/independent agent to be an authorized Indian Agent for dealing with local\/foreign drugs and cosmetics must have a manufacturing license from the <strong><em>Central Drugs Standard Control Organisations (CDSCO)<\/em><\/strong>. The application for the <a href=\"https:\/\/corpbiz.io\/manufacturing-drug-license\"><strong>manufacturing drug License<\/strong><\/a> of medical devices in India is made according to <strong><em>Rule 27<\/em><\/strong> to the State Drug Licensing Authority, CDSCO Zonal\/Sub-zonal Office, and Drugs Controller General in India CDSCO (HQ).<\/p>\n\n\n\n<p>Manufacturing of notified medical devices under Central License Approving Authority (CLAA) for sale in India, a manufacturing drug license in <strong><em>form- 28<\/em><\/strong> is required under Drugs and Cosmetics Rules. Rule 76 of Drugs and Cosmetics describe the information\/data required for a grant of a manufacturing drug license. Manufacture for sale of Disposable Hypodermic Syringes, Needles, and Disposable Perfusion sets and in-virto Diagnostic Devices are regulated by the concerned State Drug Licensing Authority.&nbsp; <\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter is-resized\"><img decoding=\"async\" src=\"https:\/\/corpbiz.io\/learning\/wp-content\/uploads\/2020\/05\/image-88.png\" alt=\"Types of Drug License\" class=\"wp-image-9006\" width=\"566\" height=\"415\" srcset=\"https:\/\/corpbiz.io\/learning\/wp-content\/uploads\/2020\/05\/image-88.png 602w, https:\/\/corpbiz.io\/learning\/wp-content\/uploads\/2020\/05\/image-88-300x220.png 300w\" sizes=\"(max-width: 566px) 100vw, 566px\" \/><\/figure><\/div>\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\/how-to-get-a-manufacturing-license-of-drugs-in-india\/#Manufacturing_License_for_Sales_or_Distribution_of_drugs\" >Manufacturing License\nfor Sales or Distribution of drugs<\/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\/how-to-get-a-manufacturing-license-of-drugs-in-india\/#Manufacturing_Licenses_and_Forms\" >Manufacturing Licenses and Forms<\/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\/how-to-get-a-manufacturing-license-of-drugs-in-india\/#Manufacture_and_Import_of_Drugs\" >Manufacture and Import\nof Drugs<\/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\/how-to-get-a-manufacturing-license-of-drugs-in-india\/#License_to_stock_sell_exhibit_or_offer_for_sale_or_distribute_the_drugs\" >License to stock, sell,\nexhibit or offer for sale or distribute the drugs.<\/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\/how-to-get-a-manufacturing-license-of-drugs-in-india\/#Procedure_to_obtain_Drug_Manufacturing_License_Fresh\" >Procedure to obtain\nDrug Manufacturing License (Fresh)<\/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\/how-to-get-a-manufacturing-license-of-drugs-in-india\/#Documents_with_Application_for_Grant_of_Drug_Manufacturing_License\" >Documents with\nApplication for Grant of Drug Manufacturing License:-<\/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\/how-to-get-a-manufacturing-license-of-drugs-in-india\/#Procedure_for_Retention_of_Drug_Manufacturing_License\" >Procedure for Retention\nof Drug Manufacturing License<\/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\/how-to-get-a-manufacturing-license-of-drugs-in-india\/#Conclusion\" >Conclusion<\/a><\/li><\/ul><\/nav><\/div>\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Manufacturing_License_for_Sales_or_Distribution_of_drugs\"><\/span>Manufacturing License\nfor Sales or Distribution of drugs<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>The <a href=\"https:\/\/corpbiz.io\/drug-license\"><strong>Drug license<\/strong><\/a> for the manufacture for sale or distribution of drugs (as specified by the Central Government from time to time by notification in Official Gazette) is granted by the Central License Approving Authority (ClAA). For the other drugs, application for grant or for renewal of the license to manufacture for sale or for distribution is required to be made to the licensing authority, which is appointed by the State Government.&nbsp; <\/p>\n\n\n\n<p>It is also noted that drugs can also be manufactured by obtaining a loan license under the Act and Rules framed. According to Rule 69A of the Rules, a loan license means a license which the licensing authority can issue to an applicant who intends to avail the manufacturing facilities owned by a licensee under the Form 25A. The license to manufacture for sale or distribution of drugs remains valid for a period of 5 years unless sooner suspended or cancelled by the licensing authority.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Manufacturing_Licenses_and_Forms\"><\/span>Manufacturing Licenses and Forms<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<table class=\"table table-bordered\">\n<tbody>\n<tr>\n<td width=\"111\">\n<p><strong>License Name<\/strong><\/p>\n<\/td>\n<td width=\"227\">\n<p><strong>Description<\/strong><\/p>\n<\/td>\n<td width=\"76\">\n<p><strong>Relevant Rule<\/strong><\/p>\n<\/td>\n<td width=\"94\">\n<p><strong>Licensing Authority <\/strong><\/p>\n<\/td>\n<td width=\"104\">\n<p><strong>Timeline<\/strong><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td width=\"111\">\n<p>Test License For Manufacturing<\/p>\n<\/td>\n<td width=\"227\">\n<p><strong><em>Form-29<\/em><\/strong> is a license to manufacture drugs for the purpose of Examination Testing and Analysis.<\/p>\n<p>The application made in <strong><em>Form-30, <\/em><\/strong>and the certificate is valid for one year.<\/p>\n<p>The applicant cannot manufacture activity other than examination, testing, and analysis purpose in the proposed manufacturing site.<\/p>\n<\/td>\n<td width=\"76\">\n<p>Rule- 89<\/p>\n<\/td>\n<td width=\"94\">\n<p>DGCI<\/p>\n<\/td>\n<td width=\"104\">\n<p>Usually between three months to six months<\/p>\n<\/td>\n<\/tr>\n<tr>\n<td width=\"111\">\n<p>Permission to Manufacture Post Successful Clinical Trial<\/p>\n<\/td>\n<td width=\"227\">\n<p>A license in <strong><em>Form-46<\/em><\/strong> is granted when an application is made in <strong><em>Form-44<\/em><\/strong> to allow manufacturing for sale of medical devices that are new in the Indian market without conducting clinical trials.<\/p>\n<\/td>\n<td width=\"76\">\n<p>Rule- 122 B<\/p>\n<\/td>\n<td width=\"94\">\n<p>DGCI<\/p>\n<\/td>\n<td width=\"104\">\n<p>6 months<\/p>\n<\/td>\n<\/tr>\n<tr>\n<td width=\"111\">\n<p>License to Manufacture Notified Medical Devices<\/p>\n<\/td>\n<td width=\"227\">\n<p>Manufacturing of notified medical devices for sale in India is given In <strong><em>Form-28<\/em><\/strong> with an application made in <strong><em>Form-27<\/em><\/strong>. It is required for the manufacturing of Disposable Hypodermic Syringes, Needles, and Disposable Perfusion sets.<\/p>\n<\/td>\n<td width=\"76\">\n<p>Rule 76<\/p>\n<\/td>\n<td width=\"94\">\n<p>For certain specified notified medical devices- DGCI.<\/p>\n<p>For other State Drug Licensing<\/p>\n<p>Authority.<\/p>\n<\/td>\n<td width=\"104\">\n<p>Usually, three months to six months.<\/p>\n<\/td>\n<\/tr>\n<tr>\n<td width=\"111\">\n<p>Loan License (Manufacture in a facility owned by third party)<\/p>\n<\/td>\n<td width=\"227\">\n<p>Manufacturing of notified device in the third party site requires a loan license in <strong><em>Form-25 A<\/em><\/strong> and <strong><em>Form-28 A<\/em><\/strong>. The license is granted by State Authority while other notified devices come under the CDSCO.<\/p>\n<\/td>\n<td width=\"76\">\n<p>Rule- 69A and<\/p>\n<p>Rule- 76A<\/p>\n<\/td>\n<td width=\"94\">\n<p>For certain specified notified medical devices- DGCI.<\/p>\n<p>For other State Drug Licensing<\/p>\n<p>Authority.<\/p>\n<\/td>\n<td width=\"104\">\n<p>Usually, three months to six months.<\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Manufacture_and_Import_of_Drugs\"><\/span>Manufacture and Import\nof Drugs<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>It is a\nmandate of the Act and Rules framed thereunder that <strong><em>no new drug shall be imported or\nmanufactured for sale unless it is approved by the Licensing Authority<\/em><\/strong> (including\nFixed-Dose Combination of two or more drugs). The term &#8216;new drug&#8217; is defined\nunder the Rule 122E of the Rules. It is provided in Rule 122E that a new drug\nmust continue considered to be a new drug for a period of four years from the\ndate of its first sanctioned approval.<\/p>\n\n\n\n<p>(CDSCO) the Central Drugs Standard Control Organisation, is a Licensing Authority for approval of the manufacturing and import of new drugs. Apart from the manufacturing and import of new drugs, any person who intends to import drugs into India, such person requires to obtain a Registration Certificate and <a href=\"https:\/\/corpbiz.io\/learning\/import-license-of-drugs-and-cosmetics-in-india\/\"><strong>Import License<\/strong><\/a> from the Licensing Authority in the manner as specified under Part-IV of the Rules. The regulatory compliances are not only restricted to drugs, but they also apply to manufacture sites based overseas, as well.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"License_to_stock_sell_exhibit_or_offer_for_sale_or_distribute_the_drugs\"><\/span>License to stock, sell,\nexhibit or offer for sale or distribute the drugs.<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>Any person or entity who intends to sell stock or distribute drugs, such person or entity is required to obtain the licenses from State Drugs Authorities. Licenses to sell and distribution of drugs are categorized mainly in categories as retail drug license, <a href=\"https:\/\/corpbiz.io\/wholesale-drug-license\"><strong>wholesale drug license<\/strong><\/a>, and restricted licenses. There are some conditions attached to every license. Therefore, the license holder has to observe such conditions during the existence of licenses. In case of any failure by the license holder to meet the conditions of licenses, the relevant licensing authority has empowered to suspend or cancel those licenses under the specified Act and Rules. It is important to note that in the event of any change in the constitution of a firm operating under the license, such a firm is required to inform the licensing authority in writing. Such license must be deemed to be valid for a maximum period of three months from the date on which the change takes place.<\/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\/apply-for-wholesale-drug-license-in-india\/\">How one can apply for Wholesale Drug License in India?\n<\/a><\/mark><\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Procedure_to_obtain_Drug_Manufacturing_License_Fresh\"><\/span>Procedure to obtain\nDrug Manufacturing License (Fresh)<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p><strong>Stage 1<\/strong>: The Applicant has to apply online to the State <strong>Drugs Controller \u2013cum- Licensing Authority of the State<\/strong><sup><a href=\"https:\/\/cdsco.gov.in\/opencms\/opencms\/en\/State-Drugs-Control\/\"><strong>[1]<\/strong><\/a><\/sup>. The documents have to be uploaded and to be handed over to the Inspecting Officer\/Drug Control Officer during the inspection. The applicant is required to make an application in the requisite Form. The details of Forms and necessary fees are mention below:-<\/p>\n\n\n\n<ul><li>Application on Form 24 for Non-biological drugs manufacturing license with a fee of Rs. 7500 for ten items per category and Rs. 300 per item for more than 10 products per category and application on Form 27 for manufacturing of a Biological drugs with a fee of Rs. 7500 for ten items per category and Rs. 300 per item for items more than 10 items per category.<\/li><li>Application on Form 24A for loan drugs manufacturing license for Non-biological drugs as per conditions prescribed and application for loan license of bio-logical drugs is to be submitted on Form 27A.<\/li><li>Application on Form 24B for repacking of license with a fee of Rs. 700 up to 10 items per category and Rs. 100 per item if the items are more than 10 items.<\/li><li>Application on Form 24C for Homeopathic manufacturing drug license with a fee of Rs. 300 for mother tincture Rs. 300 for potentized preparations and Rs. 300 for potentized and Rs. 50 for additional items if the items are more than 10. <\/li><\/ul>\n\n\n\n<p>User has option to pay the fee online through Net Banking\/Debit Card\/Credit Card and can also download the challan and can pay the fees.<\/p>\n\n\n\n<p><strong>Stage 2: <\/strong>The applicant\nshall submit an application through online mode after completing to the State\nDrugs Controller, i.e., licensing authority along with all required documents.\nApplication form is scrutinized, and the application is then forwarded to the\nSenior Drugs Control Officer of the concerned zone for inspection of the\npremises of the firm. Premises are inspected by Senior Drugs Control Officer of\nthe concerned zone, and the report is forwarded by Senior Drugs Control Officer\nalong with his recommendation to State Drugs Controller.&nbsp; <\/p>\n\n\n\n<p><strong>Stage 3: Grant of Manufacturing drug License &#8211; <\/strong>If all conditions as prescribed by the Act have complied, the license is granted by State Drugs Controller, and the applicant gets information through SMS \/email.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Documents_with_Application_for_Grant_of_Drug_Manufacturing_License\"><\/span>Documents with\nApplication for Grant of Drug Manufacturing License:-<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<ul><li>Required application form has\nto be filled Online.<\/li><li>Blueprint along with site plan\nof the premises, duly signed by the firm&#8217;s Proprietor\/partner\/Director.<\/li><li>Rent receipt or lease deed of\nthe premises (original or attested photocopies)<\/li><li>Attested copy of the\npartnership deed in case of partnership firm or Memorandum (MOA) and Article of\nAssociation (AOA) if it is Limited firm or company duly signed by Directors.<\/li><li>List of present directors\nshowing their complete name and residential address.<\/li><li>If there is change in Directors\n(registration, addition, replacement) as original with their attested photocopy\nof Form 32 in respect of such outgoing or incoming director. <\/li><li>Full details of the competent\ntechnical staff \/registered persons along with copies of their educational qualification,\nexperience, and registration certificates.<\/li><li>Non-conviction affidavit of\napproved technical staff as required with academic qualification &amp;\napproval. <\/li><li>Attested copies of academic\nqualification and the approval of technical staff as per conditions prescribed\nin Drugs and Cosmetics Act, 1940 and Rules, 1945.<\/li><li>List of the machinery <\/li><li>List of the lab equipment <\/li><li>Purchase bills of the machinery\nand equipments (original or attested photocopies)<\/li><li>NOC of fire fighting and NOC of\npollution control if applicable (original or attested photocopy)<\/li><li>Proof of load sanction\n(original or attested photocopy)<\/li><li>Attested photocopy of\nallotment\/occupation certificate form<\/li><li>Declaration in the form of\naffidavit about sleeping\/active partner\/Director responsible for day to day\nwork and conduct of the company along with declaration as to whether such\nprop\/partner\/director has been convicted under Drugs and Cosmetics Act, 1940\nand Rules, 1945. <\/li><li>Resolution of Board of\nDirectors regarding the appointment of authorised signatory.<\/li><li>Non-conviction affidavit by\nauthorised signatory, if appointed any by the firm. <\/li><\/ul>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Procedure_for_Retention_of_Drug_Manufacturing_License\"><\/span>Procedure for Retention\nof Drug Manufacturing License<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<ul><li>Government by vide its\nnotification no. GSR-1337 dated 27.10.2017 has removed the word\n&#8220;Renewal&#8221; and instead of renewal procedure of license retention by\nthe licensee, &#8220;if the licensee deposits a license retention fee before the\nexpiry of a period of every succeeding five years from the date of its issue,\nunless, it is suspended or cancelled by the Licensing Authority.<\/li><li>The license retention fee must\nbe equivalent to the respective fee required for the grant of such license,\nexcluding the inspection fee paid for grant of license.<\/li><li>In case the licensee fails to\npay license retention fee on or before the due date, he must be liable to pay\nlicense retention fee along with a late fee calculated at the rate of two\npercent of the license fee for every month or part thereof up to six months,\nand in event of the non-payment of such fee, the license must be deemed to have\nbeen cancelled. <\/li><li>Licensee at the time of\nsubmission of license retention fee must also submit an undertaking that is (a)\nthere is no change in the constitution (b) there is no change in premises (c)\nthere is no change in approved technical staff (d) list of already approved\nitems and required fee which firm intends to retain.<\/li><li>Validity certificate on receipt\nof license retention fee must be issued forthwith if full fee in all respect is\ndeposited.<\/li><\/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>A <a href=\"https:\/\/corpbiz.io\/due-diligence\"><strong>due diligence<\/strong><\/a> is required to be undertaken by every company and entity prior to entering into the Indian Pharmaceutical Industry. It must be ensured whether the prospective drug or formulation (either to be manufactured or imported to India), as qualified as a drug or a new drug since there are different set of rules and procedures for drugs that are prevailing in the Indian market for more than 4 years for new drugs. Timelines for renewal of license plays a significant role. For instance, if an application for the renewal of a drug manufacturing license is made before its expiry or if the application is made within 6 months of its expiry (after payment of additional fees), the license continues to be in force until orders are passed on the application.<\/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\/complete-overview-on-drug-license-rules-in-india\/\">A Complete Overview on Drug License Rules in India<\/a><\/mark><\/p>\n","protected":false},"excerpt":{"rendered":"<p>The company\/distributor\/independent agent to be an authorized Indian Agent for dealing with local\/foreign drugs and cosmetics must have a manufacturing license from the Central Drugs Standard Control Organisations (CDSCO). The application for the manufacturing drug License of medical devices in India is made according to Rule 27 to the State Drug Licensing Authority, CDSCO Zonal\/Sub-zonal [&hellip;]<\/p>\n","protected":false},"author":10,"featured_media":9014,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[223],"tags":[582],"acf":{"service_id":"98"},"authorName":"Soumya Bajpai","authorImageUrl":"https:\/\/corpbiz.io\/learning\/wp-content\/uploads\/2020\/01\/0.jpg","authorDescription":"Soumya has done LLB (Hons) and has a 2+years experience in writing. Her main interest is in reading judgments, new enactments and amendments taking around in law. She always strives to bring the best to work that she does.","postViews":68487,"readingTime":7,"_links":{"self":[{"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/posts\/9005"}],"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\/10"}],"replies":[{"embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/comments?post=9005"}],"version-history":[{"count":18,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/posts\/9005\/revisions"}],"predecessor-version":[{"id":23094,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/posts\/9005\/revisions\/23094"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/media\/9014"}],"wp:attachment":[{"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/media?parent=9005"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/categories?post=9005"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/tags?post=9005"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}