{"id":53520,"date":"2023-03-17T15:49:19","date_gmt":"2023-03-17T10:19:19","guid":{"rendered":"https:\/\/corpbiz.io\/learning\/?p=53520"},"modified":"2023-03-18T10:34:28","modified_gmt":"2023-03-18T05:04:28","slug":"role-of-person-responsible-for-regulatory-compliance-prrc","status":"publish","type":"post","link":"https:\/\/corpbiz.io\/learning\/role-of-person-responsible-for-regulatory-compliance-prrc\/","title":{"rendered":"Role of Person Responsible For Regulatory Compliance (PRRC) \u2013 A Complete Analysis"},"content":{"rendered":"\n<p>PRRC is an acronym that stands for\nthe person responsible for regulatory compliance. It is one of the new\nrequirements of the European Union&#8217;s Medical Device Regulation (MDR) &amp;\nIn-Vitro Diagnostic Medical Device Regulation (IVDMDR) (IVDR). Its goal is to\nensure that businesses have access to a qualified regulatory expert.<\/p>\n\n\n\n<p>Article 15 of the EU MDR &amp; EU\nIVDR requires manufacturers (and authorized representatives) to have at least a\nperson responsible for regulatory compliance on staff to ensure the company is\nin complies with the MDR\/IVDR. This requirement is mandatory as of the\neffective date of the respective EU Regulation, which is May 26, 202, for the\nMDR and May 26, 2022, for the IVDR.<\/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\/role-of-person-responsible-for-regulatory-compliance-prrc\/#What_is_PRRC\" >What is PRRC?<\/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\/role-of-person-responsible-for-regulatory-compliance-prrc\/#Who_Can_Be_Person_Responsible_For_Regulatory_Compliance_PRRC\" >Who Can Be Person Responsible For Regulatory Compliance (PRRC)?<\/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\/role-of-person-responsible-for-regulatory-compliance-prrc\/#Who_Needs_A_Person_Responsible_For_Regulatory_Compliance_PRRC\" >Who Needs A Person Responsible For Regulatory Compliance (PRRC)?<\/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\/role-of-person-responsible-for-regulatory-compliance-prrc\/#Can_A_Company_Have_More_Than_One_PRRC\" >Can A Company Have More Than One PRRC?<\/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\/role-of-person-responsible-for-regulatory-compliance-prrc\/#Appointment_of_Person_Responsible_For_Regulatory_Compliance_PRRC\" >Appointment of Person Responsible For Regulatory Compliance (PRRC)<\/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\/role-of-person-responsible-for-regulatory-compliance-prrc\/#Importance_of_Identifying_PRRC\" >Importance of Identifying PRRC<\/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\/role-of-person-responsible-for-regulatory-compliance-prrc\/#Responsibilities_of_A_PRRC_under_the_MDR\" >Responsibilities of A PRRC under the MDR<\/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\/role-of-person-responsible-for-regulatory-compliance-prrc\/#Responsibilities_of_A_PRRC_under_the_IVDR\" >Responsibilities of A PRRC under the IVDR<\/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\/role-of-person-responsible-for-regulatory-compliance-prrc\/#PRRC_Outsourcing\" >PRRC Outsourcing<\/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\/role-of-person-responsible-for-regulatory-compliance-prrc\/#Liabilities_of_the_PRRC\" >Liabilities of the PRRC<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-11\" href=\"https:\/\/corpbiz.io\/learning\/role-of-person-responsible-for-regulatory-compliance-prrc\/#Conclusion\" >Conclusion<\/a><\/li><\/ul><\/nav><\/div>\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"What_is_PRRC\"><\/span>What is PRRC?<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>PRRC is an acronym for &#8220;Person\nResponsible for Regulatory Compliance&#8221;.<sup> <\/sup>The EUMDR introduces new\nrequirements for <strong><a class=\"text-primary\" href=\"https:\/\/corpbiz.io\/learning\/opportunities-in-indian-medical-device-manufacturing\/\">medical device manufacturers<\/a><\/strong> and clarifies the roles of PRRC.\nAccording to the new EU MDR regulation, which went into effect on May 26, 2021,\nmedical device manufacturers must have a PRRC to ensure regulatory compliance.\nPRRCs play critical roles and responsibilities in the establishment of medical\ndevice manufacturing plants.<\/p>\n\n\n\n<p>The PRRCs are the authorized\nindividuals who must have specific qualifications and experience. The EU has\npublished new rules and regulations for medical device manufacturers, and these\ncompanies or organizations should have Person Responsible for Regulatory\nCompliance (PRRC) with them to investigate regulations and policies. PRRC is in\ncharge of regulatory compliance. Article 15(1) of the MDR and IVDR outlines\nsome specific requirements for PRRC. If a medical device manufacturer wants to\nsell or supply their device in the European Union, they must have at least one\nPerson Responsible for Regulatory Compliance (PRRC) on site.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Who_Can_Be_Person_Responsible_For_Regulatory_Compliance_PRRC\"><\/span>Who Can Be Person Responsible For Regulatory Compliance (PRRC)?<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>The Person Responsible for\nRegulatory Compliance (PRRC) can be any person who has the necessary expertise\nin the field of medical devices, as demonstrated by the qualifications listed\nbelow.<\/p>\n\n\n\n<ul><li>The individual must have a Diploma\nor University Degree in Law, Medicine, Pharmacy, Engineering, or another\nrelevant discipline recognized by the member state, as well as at least one\nyear of experience in Medical Device Quality Management.<\/li><\/ul>\n\n\n\n<p>Or&nbsp;<\/p>\n\n\n\n<ul><li>Four years of professional experience\nin regulatory affairs or Quality Management systems for Medical Devices.<\/li><\/ul>\n\n\n\n<p>If you are a manufacturer of\ncustom-made devices, you may demonstrate the necessary expertise by having at\nleast two years of professional experience in a relevant field of manufacturing,\nsubject to national provisions regarding professional qualifications. If a\nmanufacturer does not have someone who meets the above requirements, they can:<\/p>\n\n\n\n<ul><li>Hire a new employee to fill this role.<\/li><li>Hire a consultant for a set period while\nsimultaneously training your current employee.<\/li><\/ul>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Who_Needs_A_Person_Responsible_For_Regulatory_Compliance_PRRC\"><\/span>Who Needs A Person Responsible For Regulatory Compliance (PRRC)?<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>A PRRC is required for all manufacturers and EU-authorized representatives. Manufacturers must confirm that their EU-authorized representative has appointed someone who satisfies the Person Responsible for Regulatory Compliance (PRRC) qualifications outlined in Article 15. If a company is made up of more than one legal manufacturer, each one must appoint its PRRC.<\/p>\n\n\n\n<p>According to the MDCG 2019-07\ndocument, the PRRC&#8217;s new role adds a level of scrutiny and ensures that the\nmandatory activities related to manufacturing supervision and control, as well\nas post-market surveillance and vigilance, are carried out appropriately. To\neffectively achieve this additional level, one person cannot serve as both the Person\nResponsible for Regulatory Compliance (PRRC) for a manufacturer outside the EU\nand the company&#8217;s EU-authorized representative. In this manner, if a\nmicro\/small business outsources its PRRC to an external organization, the\ncompany&#8217;s authorized representative cannot outsource their Person Responsible\nfor Regulatory Compliance (PRRC) to the same outside expert.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Can_A_Company_Have_More_Than_One_PRRC\"><\/span>Can A Company Have More Than One PRRC?<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>Companies are not limited to only\none Person Responsible for Regulatory Compliance (PRRC), and responsibilities\ncan be assigned to multiple people as long as the qualification requirements\nare met and the distribution of respective areas of responsibility is\ndocumented in writing (Article 15[4<strong>]<\/strong>).\nIf the responsibilities are divided among several people, make certain that all\nresponsibilities are covered.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Appointment_of_Person_Responsible_For_Regulatory_Compliance_PRRC\"><\/span>Appointment of Person Responsible For Regulatory Compliance (PRRC)<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>The PRRC is appointed in the same\nway that your management representative is. You must create and sign an\nagreement with the Person Responsible for Regulatory Compliance (PRRC) that\nincludes the following information:<\/p>\n\n\n\n<ul><li>Purpose<\/li><li>Scope<\/li><li>Qualification Requirement<\/li><li>PRRC Roles And Responsibilities&nbsp;<\/li><li>Any Additional Roles And Responsibilities&nbsp;<\/li><li>The PRRC And Company Head&#8217;s Signature and Date.&nbsp;<\/li><\/ul>\n\n\n\n<p>The manufacturer must ensure that Person\nResponsible for Regulatory Compliance (PRRC) is not penalized within the\nmanufacturer&#8217;s organization for performing his or her duties properly,\nregardless of whether or not they are an employee of the organization. The\nmanufacturer should be aware that only a qualified representative can act as Person\nResponsible for Regulatory Compliance (PRRC).<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Importance_of_Identifying_PRRC\"><\/span>Importance of Identifying PRRC<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>Identifying the PRRC for your\norganization is a critical requirement that applies to the European Union and\nis a core area of responsibility for a person or people under the medical\ndevice regulation, also known as the In vitro device regulation. The decision\nto appoint the PRRC is also influenced by the size of the organization. Under\nthe new EU MDR, this is a mandatory requirement for any <strong><a class=\"text-primary\" href=\"https:\/\/corpbiz.io\/ce-certification\">CE Marking<\/a><\/strong>.<\/p>\n\n\n\n<p>The object of this identification is\nto have a qualified regulatory expert who is responsible directly for\nmanufacturing as well as market surveillance and reporting systems to ensure\nthat the company meets European Union requirements. Companies are not limited\nto only one PRRC, and responsibilities can be assigned to multiple people as\nlong as the qualification requirements are met &amp; the distribution of the\nspecific areas of responsibility is documented. If the responsibilities are divided\namong several people, make certain that all responsibilities are covered.<\/p>\n\n\n\n<p>The Regulations express a clear\ndesire to add another level of scrutiny to the supervision and control of\nmedical device manufacturing, as well as relevant post-market surveillance and\nvigilance activities. As a result, identifying the PRRC role is a sole position\nfrom the European Union Authorized Representative. The importance of the MDR\nand IVDR identifying the PRRC role extends beyond the role of a safety officer.\nMDCG 2019-7 provides PRRC with prescriptive guidance on qualification and\nresponsibility. The manufacturer must find someone who can fill this critical\nrole.<\/p>\n\n\n\n<p>The PRRC should be identified if he\nis in charge of the technical documentation EU Declaration of Conformity (drawn\nup and kept up to date), post-market surveillance obligations, and checking the\nconformity of devices before they are released (according to the QMS). Each\nlegal manufacturer is required to have its PRRC. If the manufacturer is located\nin the EU, the PRRC must be close to it also. Both must be closer to each\nother.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Responsibilities_of_A_PRRC_under_the_MDR\"><\/span>Responsibilities of A PRRC under the MDR<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>The PRRC is responsible for ensuring\nthe followings according to article 15(3), EU MDR:&nbsp;<\/p>\n\n\n\n<p><strong>(a)<\/strong> Prior to the release of a device, the conformity of the devices should be checked properly in the line with the quality management system under which the devices are manufactured;&nbsp;<\/p>\n\n\n\n<p><strong>(b)<\/strong> The technical documentation &amp; the EU declaration of conformity are to be prepared and kept up to date; and<\/p>\n\n\n\n<p><strong>(c)<\/strong> The post-market surveillance obligations are met following Article 10(10).<\/p>\n\n\n\n<p><strong>(d)<\/strong> The reporting obligations referred to in Articles 87-91 are met (NOTE: This refers to Vigilance reporting, which includes serious incidents, field safety corrective action, and incident trend reporting).<\/p>\n\n\n\n<p><strong>(e)<\/strong> The statement referred to in Section 4.1 of Chapter II of Annex XV is issued in the case of investigational devices. NOTE: This is the statement confirming that the investigational device complies with the General Safety &amp; Performance Requirements in Annex I of the EU Medical Device Rules, except those relating to aspects covered by the clinical investigation, and that precautions are taken to safeguard the subject&#8217;s health &amp; safety.<\/p>\n\n\n\n<p>The responsibility of a PRRC of an authorized\nrepresentative (who is subject to the same qualification requirements as a PRRC\nof a manufacturer) under the MDR is to ensure compliance with the requirements\napplicable to the EU authorized representative, as outlined in Article 11(3) of\nthe Medical Device Rules.<\/p>\n\n\n\n<p>The MDR requires the name and\ncontact information of the designated person responsible for regulatory\ncompliance to be entered into the EUDAMED database.<\/p>\n\n\n\n<p>The MDR does not require the PRRC to\nperform all tasks and activities to ensure compliance with the requirements,\nbut only those that fall under his\/her responsibility.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Responsibilities_of_A_PRRC_under_the_IVDR\"><\/span>Responsibilities of A PRRC under the IVDR<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>The PRRC is responsible for ensuring\nthe followings according to article 15(3), EU IVDR:&nbsp;&nbsp;<\/p>\n\n\n\n<p><strong>(a)<\/strong> Prior to the release of a device, the\nconformity of the devices should be checked properly in the line with the\nquality management system under which the devices are manufactured;&nbsp;<\/p>\n\n\n\n<p><strong>(b)<\/strong> The technical documentation &amp; the EU\ndeclaration of conformity are prepared and kept up to date;<\/p>\n\n\n\n<p><strong>(c)<\/strong> The post-market surveillance obligations are\nmet per Article 10(9); and<\/p>\n\n\n\n<p><strong>(d)<\/strong> The reporting obligations referred to in\nArticles 82-86 are met (NOTE: This refers to Vigilance reporting, which\nincludes serious incidents, field safety corrective action, and incident trend\nreporting).<\/p>\n\n\n\n<p><strong>(e)<\/strong> The statement referred to in Section 4.1 of\nChapter II of Annex XV is issued in the instance of devices for performance\nstudies intended to be used concerning interventional clinical performance\nstudies\/other performance studies involving risks for the subjects.<\/p>\n\n\n\n<p>This is the statement confirming\nthat the device meets the General Safety and Performance Requirements in Annex\nI of the EU IVDR, except for aspects covered by the clinical performance study\n&amp; that precautions are taken to protect the subject&#8217;s health and safety.<\/p>\n\n\n\n<p>The European Union Medical Device\nCoordination Group clarifies in its guidance document <strong>MDCG 2019-7<\/strong><sup><a class=\"text-primary\" href=\"https:\/\/health.ec.europa.eu\/system\/files\/2020-09\/md_mdcg_2019_7_guidance_art15_mdr_ivdr_en_0.pdf\"><strong>[1]<\/strong><\/a><\/sup>, as it does for the MDR\nthat the responsibilities of an EU-authorized representative&#8217;s PRRC are to\nensure the fulfillment of the EU-authorized representative duties, as stated in\nthe manufacturer&#8217;s mandate and accordance with Article 11(3) of the IVDR.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"PRRC_Outsourcing\"><\/span>PRRC Outsourcing<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>Only companies with fewer than 50 employees and an annual turnover of less than EUR 10 million (defined as micro and small enterprises under Commission Recommendation 2003\/361\/EC) are permitted to outsource their PRRC to an outside expert, provided that the PRRC meets the qualification criteria and is permanently and continuously available to them.<\/p>\n\n\n\n<p>It is vital to note that neither the\nMDR\/IVDR nor the MDCG 2019-7 guidance document goes into detail about the\npractical implications of permanent and continuous availability. As a result,\nit is recommended that manufacturers and EU-authorized representatives\ninterpret this requirement conservatively and that their external PRRC is\nreachable 24 hours a day, seven days a week &amp; has an officially designated\ndesignee for absences. The contractual agreement with the Person Responsible\nfor Regulatory Compliance (PRRC) should detail his or her permanent &amp;\ncontinuous availability, as well as the qualification of the relevant person.<\/p>\n\n\n\n<p>Because the person will be\nresponsible for compliance with procedures, technical documentation, and\npost-market obligations, outsourcing the PRRC function necessitates appropriate\nagreements. An outsourced PRRC must be available at all times and integrated in\nsuch a way that all parties involved can meet the MDR\/IVDR requirements.<\/p>\n\n\n\n<p>In terms of PRRC location, the MDCG\ndocument specifies that a PRRC of manufacturers located in the European Union\nmust also be located in the EU. This is because a permanent and continuous link\nbetween the PRRC and the manufacturing activities must be established.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Liabilities_of_the_PRRC\"><\/span>Liabilities of the PRRC<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>While the MDR\/IVDR states that the\nPRRC must not be discriminated against because of their duties, it does not go\ninto detail about the person responsible for regulatory compliance&#8217;s potential\nliability. Neither does the MDCG recommendation (MDCG 2019-7). However, this\ninformation would be useful in ensuring that the PRRC doesn&#8217;t suffer any\ndisadvantage in carrying out its duties and in structuring the mandate\naccordingly. While some of these points (such as liability limitations) can be\nincluded in employment contracts, national laws will have to clarify these\npoints until an EU-wide provision is in place.<\/p>\n\n\n\n<p>The question remains whether a\nviolation of Article 15(3) will result in enforcement directed against the\ncompany\/also against the PRRC &amp; to what extent and under what circumstances\n(such as gross negligence, serious fault, or fraud) a PRRC can be punished for\nfailing to carry out his responsibilities as outlined in Article 15(3).<\/p>\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>TEAM-PRRC is a European non-profit organization formed to represent its members at the European Commission and the Medical Device Coordination Group. The association&#8217;s goal is to gain insight into and influence the PRRC role guidance that is being developed, as well as to promote understanding of the PRRC responsibilities. TEAM-PRRC will assist its members by analyzing available guidance and promoting greater security for the PRRC professionals themselves, as the role carries significant responsibility and potentially significant personal liability.<\/p>\n\n\n\n<p><strong>Also Read<\/strong>: <br><a href=\"https:\/\/corpbiz.io\/learning\/how-has-eu-mdr-affected-ce-marking-for-medical-devices\/\">How Has EU-MDR Affected CE Marking For Medical Devices?<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>PRRC is an acronym that stands for the person responsible for regulatory compliance. It is one of the new requirements of the European Union&#8217;s Medical Device Regulation (MDR) &amp; In-Vitro Diagnostic Medical Device Regulation (IVDMDR) (IVDR). Its goal is to ensure that businesses have access to a qualified regulatory expert. Article 15 of the EU [&hellip;]<\/p>\n","protected":false},"author":50,"featured_media":53557,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[946],"tags":[3251],"acf":{"service_id":"385"},"authorName":"Arya Panda","authorImageUrl":"https:\/\/corpbiz.io\/learning\/wp-content\/uploads\/2023\/02\/MicrosoftTeams-image-107.jpg","authorDescription":"Arya is a law graduate from ICFAI University, Dehradun and when it comes to his academics, he has always been a responsible, inquisitive, and enthusiastic learner. He is extremely passionate about writing, a\u00a0skilled researcher, and has a great flair for drafting. Arya has got himself acquainted with various aspects of law while working as an intern with several prominent law firms. His primary interests lie in Corporate, IPR, and Arbitration. His work experience, strong work ethic, head for law, and passion for working as a lawyer to change the world by helping to implement justice are what he brings to the opportunity with any office.\u00a0","postViews":2736,"readingTime":8,"_links":{"self":[{"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/posts\/53520"}],"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\/50"}],"replies":[{"embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/comments?post=53520"}],"version-history":[{"count":3,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/posts\/53520\/revisions"}],"predecessor-version":[{"id":53559,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/posts\/53520\/revisions\/53559"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/media\/53557"}],"wp:attachment":[{"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/media?parent=53520"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/categories?post=53520"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/tags?post=53520"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}