{"id":15520,"date":"2020-08-29T12:47:16","date_gmt":"2020-08-29T07:17:16","guid":{"rendered":"https:\/\/corpbiz.io\/learning\/?p=15520"},"modified":"2020-08-29T13:53:50","modified_gmt":"2020-08-29T08:23:50","slug":"documents-required-for-ce-certification-in-india","status":"publish","type":"post","link":"https:\/\/corpbiz.io\/learning\/documents-required-for-ce-certification-in-india\/","title":{"rendered":"A Complete Overview of Documents required for CE Certification in India"},"content":{"rendered":"\n<p class=\"has-drop-cap\">Nearly every product that is sold\nin the European Union steak around a safety standard called CE. It is the short\nform of the term called &#8220;Conformit\u00e9 Europ\u00e9enne,&#8221; a french word.\nManufacturers across the EU require to affix this logo on their product to\nensure conformity against the EU\u2019s directive and regulations. The CE mark is\nsort of manufacturer\u2019s declaration that their product meets the required\ncompliances against the applicable health, safety, and environmental norms.<\/p>\n\n\n\n<p>It should be noted that any European organization does not own the CE mark.\u00a0 It is an autonomous standard with a certain set of rules and regulations that ensure the product\u2019s safety on several testing grounds. In this blog, you will come across Documents required for CE certification in India. <\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" width=\"760\" height=\"464\" src=\"https:\/\/corpbiz.io\/learning\/wp-content\/uploads\/2020\/08\/image-123.png\" alt=\"CE Certification in India\" class=\"wp-image-15534\" srcset=\"https:\/\/corpbiz.io\/learning\/wp-content\/uploads\/2020\/08\/image-123.png 760w, https:\/\/corpbiz.io\/learning\/wp-content\/uploads\/2020\/08\/image-123-300x183.png 300w\" sizes=\"(max-width: 760px) 100vw, 760px\" \/><\/figure><\/div>\n\n\n\n<p>In general, CE mark can be raised\nby the manufacturer situated in the EU. However, it is not limited to the EU\nresident as the people from an overseas location can avail of this marking by\nappointing an authorized representative in the EU. Some directives guide the\nmanufacturer to test its product by the certified third-party lab to ensure\nconformance with applicable standards. <\/p>\n\n\n\n<p>These labs are also known as notified bodies in the EU. If the applicable directives discourage Notified Body\u2019s use, then manufacturers can rely on their in-house testing facility for product conformity assessment. Each directive outline which conformity assessment procedures manufacture can undertake. Currently, you must take note that there are eight modules exist for the conformity assessment. <\/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\/know-about-the-ce-certification-process\/\">All you need to know about the CE Certification Process<\/a><\/mark><\/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\/documents-required-for-ce-certification-in-india\/#Technical_Documentation_Brief\" >Technical Documentation Brief<\/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\/documents-required-for-ce-certification-in-india\/#Technical_Document_Required_for_the_LVD_ie_Low_Voltage_Directive\" >Technical Document Required for the LVD, i.e.\nLow Voltage Directive<\/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\/documents-required-for-ce-certification-in-india\/#Technical_Document_Required_for_the_EMCD_ie_Electromagnetic_Compatibility_Directive_EMCD\" >Technical Document Required for the EMCD, i.e.\nElectromagnetic Compatibility Directive (EMCD)<\/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\/documents-required-for-ce-certification-in-india\/#EC-type_Examination_Certificate_Issuance_Criteria\" >EC-type Examination Certificate Issuance\nCriteria<\/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\/documents-required-for-ce-certification-in-india\/#Conclusion\" >Conclusion<\/a><\/li><\/ul><\/nav><\/div>\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Technical_Documentation_Brief\"><\/span>Technical Documentation Brief<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>The manufacturer must prepare the\ntechnical documentation, and it should enclose detail regarding risk assessment\nand adequate assessment. Technical documentation plays a prominent role in\nsafeguarding an organization. It will retain the information about the\nevolution of the product and the evidence regarding its conformance with the\nrequired legislation. Technical documentation encloses a wide range of\ninformation about the product, including the test report. TD doesn\u2019t follow any\nprescribed format as it could vary with regulations and directives. <\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Product Complies with the Essential Safety Requirements<\/h3>\n\n\n\n<p>All CE marking directive directs the manufacture to prepare technical documentation that declares that the product complies with the essential safety requirements. Technical documentation typically remains valid for ten years from the date on which the manufacturing of products was initiated. The updation of the technical documentation should be done accordingly as per changes in the product\u2019s component, manufacturing process, or conformity assessment procedures. Now, let\u2019s move to the main section i:e Documents required for <a href=\"https:\/\/corpbiz.io\/ce-certification\"><strong>CE certification in India<\/strong><\/a>. <\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Technical_Document_Required_for_the_LVD_ie_Low_Voltage_Directive\"><\/span>Technical Document Required for the LVD, i.e.\nLow Voltage Directive<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<ul><li>Detail of the product\u2019s design and manufacturing to assess conformity with the applicable legislation. <\/li><li>Details description of the product for which CE marking is required. <\/li><li>Schematic and drawing of the product\u2019s component, circuits, and subassemblies along with the explanations for easy understanding. <\/li><li>The functionality of the product. <\/li><li>Detail of the existing standards governing the safety aspect of the product apart from the <strong><em>harmonized standards<\/em><\/strong><sup><a href=\"https:\/\/en.wikipedia.org\/wiki\/Harmonization_(standards)\"><strong><em>[1]<\/em><\/strong><\/a><\/sup>.<\/li><li>Test report of the product generated by the notified body for the conformity assessment. <\/li><\/ul>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Technical_Document_Required_for_the_EMCD_ie_Electromagnetic_Compatibility_Directive_EMCD\"><\/span>Technical Document Required for the EMCD, i.e.\nElectromagnetic Compatibility Directive (EMCD)<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<ul><li>Product\nidentification mentioned in the technical documentation. <\/li><li>A\ndetailed description of the sample product. <\/li><li>Evidence\nregarding the existing compliances governing the safety of the product. This\nshould also cover the detailed procedure acquired by the applicant in order to\nmeet the requirement for such complancies. <\/li><li>Evidence\nregarding the European harmonized standards, if available. <\/li><li>EMC\nassessment report. <\/li><li>Declaration\nof the notified body in case if the manufacturer opted for procedure mentioned\nunder Annex III of the EMCD,<\/li><li>Test\nreport<\/li><li>Details\nof the examination carried out for the apparatus. <\/li><li>Schematics\nof the testing&nbsp; <\/li><\/ul>\n\n\n\n<h3 class=\"wp-block-heading\">Notified Body Module<\/h3>\n\n\n\n<p>The notified body does the issuance\nof an EC type-examination certificate after testing the product as per the\ndirection set out in module B to Decision 768\/2008\/EC.&nbsp; The NB\u2019s keeps a copy of the certificate for\nfuture reference. Any changes made to the production process or the product\nmust be intimated to the NB. EC type-examination enclose the following\ninformation. <\/p>\n\n\n\n<ul><li>The name and complete address of the manufactures. <\/li><li>Conclusion of the examination <\/li><li>Applicable validity conditions.<\/li><\/ul>\n\n\n\n<div class=\"shadow1\"><strong>Note:<\/strong> The manufacturer needs to review the EC-type examination certificate periodically, as mentioned in the Directive 2009\/48\/EC, Article 20.4. The certificate would no longer be valid if the product component or the manufacturing process change within the validity period. Such alternation would trigger the requirement of reassessment in order to stay in line with the required directive. <\/div>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"EC-type_Examination_Certificate_Issuance_Criteria\"><\/span>EC-type Examination Certificate Issuance\nCriteria<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<ul><li>Its issuance of this certificate depends on the\nassessment of the tested model. <\/li><li>The EC-type examination is performed by the\nnotified bodies, which eventually decides whether the product is fit to use or\nnot as per the EU\u2019s directives. The NB is the autonomous body that adheres to\nno relationship with the manufacturers seeking certification. <\/li><li>The manufacturer must streamline its production\nunit to set out conformity with the approved model seeking certification. <\/li><li>The applicant should intimate NB about the\nmanufacturing process changes without exception so that NB can conclude the\nreport accordingly. <\/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>CE marking is absolutely mandatory for the manufacture who want sold their product in EU marketplace. Undoubtedly raising a declaration for conformity against the EU\u2019s directive and regulations is an intimidating task for any manufactures. Thus; its important to cover all the basic points before diving into the conformity assessment of the product. It will help you overcome skepticism related to assessment formalities and standards.  <\/p>\n\n\n\n<p>The technical quandaries are apparent in obtaining any standard for the product. So in order to clear that hassle, make sure to feel free to connect <a href=\"https:\/\/corpbiz.io\/\"><strong>Coprbiz<\/strong><\/a> expert today. You can also intimate our expert in case of any technical information regarding Documents required for CE certification in India.  <\/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\/how-to-get-ce-marking-certification-in-india\/\">How to Get CE Marking Certification in India?<\/a><\/mark><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Nearly every product that is sold in the European Union steak around a safety standard called CE. It is the short form of the term called &#8220;Conformit\u00e9 Europ\u00e9enne,&#8221; a french word. Manufacturers across the EU require to affix this logo on their product to ensure conformity against the EU\u2019s directive and regulations. The CE mark [&hellip;]<\/p>\n","protected":false},"author":22,"featured_media":15532,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[251],"tags":[934],"acf":{"service_id":"0"},"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":9116,"readingTime":4,"_links":{"self":[{"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/posts\/15520"}],"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=15520"}],"version-history":[{"count":11,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/posts\/15520\/revisions"}],"predecessor-version":[{"id":15535,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/posts\/15520\/revisions\/15535"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/media\/15532"}],"wp:attachment":[{"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/media?parent=15520"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/categories?post=15520"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/tags?post=15520"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}