{"id":5585,"date":"2023-09-20T12:42:04","date_gmt":"2023-09-20T07:12:04","guid":{"rendered":"https:\/\/pharmaceuticalcarrier.com\/?p=5585"},"modified":"2023-09-20T12:42:14","modified_gmt":"2023-09-20T07:12:14","slug":"standard-operating-procedure-sop-for-writing-method-of-analysis-for-packaging-material","status":"publish","type":"post","link":"https:\/\/pharmaceuticalcarrier.com\/index.php\/2023\/09\/20\/standard-operating-procedure-sop-for-writing-method-of-analysis-for-packaging-material\/","title":{"rendered":"Standard Operating Procedure (SOP) for Writing Method of Analysis for Packaging Material"},"content":{"rendered":"\n<div id=\"ez-toc-container\" class=\"ez-toc-v2_0_76 counter-hierarchy ez-toc-counter ez-toc-transparent ez-toc-container-direction\">\n<div class=\"ez-toc-title-container\">\n<p class=\"ez-toc-title\" style=\"cursor:inherit\">Table of 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 ' ><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-1\" href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/2023\/09\/20\/standard-operating-procedure-sop-for-writing-method-of-analysis-for-packaging-material\/#1_Purpose_of_Writing_Method_of_Analysis_for_Packaging_Material\" >1. Purpose of Writing Method of Analysis for Packaging Material<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-2\" href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/2023\/09\/20\/standard-operating-procedure-sop-for-writing-method-of-analysis-for-packaging-material\/#2_Scope_of_Writing_Method_of_Analysis_for_Packaging_Material\" >2. Scope of Writing Method of Analysis for Packaging Material<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-3\" href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/2023\/09\/20\/standard-operating-procedure-sop-for-writing-method-of-analysis-for-packaging-material\/#3_Definitions_involved_in_Writing_Method_of_Analysis_for_Packaging_Material\" >3. Definitions involved in Writing Method of Analysis for Packaging Material<\/a><ul class='ez-toc-list-level-3' ><li class='ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-4\" href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/2023\/09\/20\/standard-operating-procedure-sop-for-writing-method-of-analysis-for-packaging-material\/#31_Packaging_Material\" >3.1 Packaging Material:<\/a><\/li><\/ul><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-5\" href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/2023\/09\/20\/standard-operating-procedure-sop-for-writing-method-of-analysis-for-packaging-material\/#4_Safety_Precautions_and_Personal_Protective_Equipment_PPE\" >4. Safety Precautions and Personal Protective Equipment (PPE)<\/a><ul class='ez-toc-list-level-3' ><li class='ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-6\" href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/2023\/09\/20\/standard-operating-procedure-sop-for-writing-method-of-analysis-for-packaging-material\/#41_PPE_Requirements\" >4.1. PPE Requirements<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-7\" href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/2023\/09\/20\/standard-operating-procedure-sop-for-writing-method-of-analysis-for-packaging-material\/#42_Chemical_Safety\" >4.2. Chemical Safety<\/a><\/li><\/ul><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-8\" href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/2023\/09\/20\/standard-operating-procedure-sop-for-writing-method-of-analysis-for-packaging-material\/#5_Equipment_and_Materials\" >5. Equipment and Materials<\/a><ul class='ez-toc-list-level-3' ><li class='ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-9\" href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/2023\/09\/20\/standard-operating-procedure-sop-for-writing-method-of-analysis-for-packaging-material\/#51_Laboratory_Equipment\" >5.1. Laboratory Equipment<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-10\" href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/2023\/09\/20\/standard-operating-procedure-sop-for-writing-method-of-analysis-for-packaging-material\/#52_Reference_Standards\" >5.2. Reference Standards<\/a><\/li><\/ul><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-11\" href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/2023\/09\/20\/standard-operating-procedure-sop-for-writing-method-of-analysis-for-packaging-material\/#6_Method_of_Analysis_Development_Procedure\" >6. Method of Analysis Development Procedure<\/a><ul class='ez-toc-list-level-3' ><li class='ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-12\" href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/2023\/09\/20\/standard-operating-procedure-sop-for-writing-method-of-analysis-for-packaging-material\/#61_Method_Development\" >6.1. Method Development<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-13\" href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/2023\/09\/20\/standard-operating-procedure-sop-for-writing-method-of-analysis-for-packaging-material\/#62_Method_Validation\" >6.2. Method Validation<\/a><\/li><\/ul><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-14\" href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/2023\/09\/20\/standard-operating-procedure-sop-for-writing-method-of-analysis-for-packaging-material\/#7_Documentation_and_Recordkeeping\" >7. Documentation and Recordkeeping<\/a><ul class='ez-toc-list-level-3' ><li class='ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-15\" href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/2023\/09\/20\/standard-operating-procedure-sop-for-writing-method-of-analysis-for-packaging-material\/#71_Method_Documentation\" >7.1. Method Documentation<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-16\" href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/2023\/09\/20\/standard-operating-procedure-sop-for-writing-method-of-analysis-for-packaging-material\/#72_Method_Validation_Records\" >7.2. Method Validation Records<\/a><\/li><\/ul><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-17\" href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/2023\/09\/20\/standard-operating-procedure-sop-for-writing-method-of-analysis-for-packaging-material\/#8_Method_Revision_and_Review\" >8. Method Revision and Review<\/a><ul class='ez-toc-list-level-3' ><li class='ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-18\" href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/2023\/09\/20\/standard-operating-procedure-sop-for-writing-method-of-analysis-for-packaging-material\/#81_Revision_Process\" >8.1. Revision Process<\/a><\/li><\/ul><\/li><\/ul><\/nav><\/div>\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"1_Purpose_of_Writing_Method_of_Analysis_for_Packaging_Material\"><\/span><strong>1. Purpose of Writing Method of Analysis for Packaging Material<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>The purpose of this Standard Operating Procedure (SOP) is to establish guidelines for the development and documentation of methods of analysis for packaging materials used within [Company Name]. This procedure ensures that methods are systematically created, validated, and maintained for quality control and compliance purposes.<\/p><div class=\"pharm-content\" id=\"pharm-2391819331\"><script async src=\"\/\/pagead2.googlesyndication.com\/pagead\/js\/adsbygoogle.js?client=ca-pub-8402705006112223\" crossorigin=\"anonymous\"><\/script><ins class=\"adsbygoogle\" style=\"display:block;\" data-ad-client=\"ca-pub-8402705006112223\" \ndata-ad-slot=\"7652789694\" \ndata-ad-format=\"auto\"><\/ins>\n<script> \n(adsbygoogle = window.adsbygoogle || []).push({}); \n<\/script>\n<\/div>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"2_Scope_of_Writing_Method_of_Analysis_for_Packaging_Material\"><\/span><strong>2. Scope of Writing Method of Analysis for Packaging Material<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>This SOP applies to all personnel involved in the development of methods of analysis for packaging materials within [Company Name]. It encompasses the procedures for method creation, validation, documentation, and revision.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"3_Definitions_involved_in_Writing_Method_of_Analysis_for_Packaging_Material\"><\/span><strong>3. Definitions involved in Writing Method of Analysis for Packaging Material<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<h3 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"31_Packaging_Material\"><\/span>3.1 <strong>Packaging Material<\/strong>: <span class=\"ez-toc-section-end\"><\/span><\/h3>\n\n\n\n<p>Materials used for the containment, protection, and preservation of pharmaceutical products, including containers, closures, and labels.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"4_Safety_Precautions_and_Personal_Protective_Equipment_PPE\"><\/span><strong>4. Safety Precautions and Personal Protective Equipment (PPE)<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<h3 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"41_PPE_Requirements\"><\/span><strong>4.1. PPE Requirements<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h3>\n\n\n\n<p>4.1.1 Personnel involved in method development and testing must wear appropriate PPE, including lab coats, safety goggles, and gloves.<\/p>\n\n\n\n<p>4.1.2 Ensure that PPE is in good condition and properly fitted.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"42_Chemical_Safety\"><\/span><strong>4.2. Chemical Safety<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h3>\n\n\n\n<p>4.2.1 Handle all chemicals and solvents involved in method development with care, following manufacturer instructions and safety data sheets.<\/p>\n\n\n\n<p>4.2.2 Store chemicals in designated areas away from incompatible substances.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"5_Equipment_and_Materials\"><\/span><strong>5. Equipment and Materials<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<h3 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"51_Laboratory_Equipment\"><\/span><strong>5.1. Laboratory Equipment<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h3>\n\n\n\n<p>5.1.1 Ensure that all laboratory equipment used for method development, such as balances, chromatography systems, and spectrophotometers, is in proper working condition and calibrated.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"52_Reference_Standards\"><\/span><strong>5.2. Reference Standards<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h3>\n\n\n\n<p>5.2.1 Ensure the availability of reference standards necessary for method development and validation.<\/p>\n\n\n\n<p>5.2.2 Reference standards should have certificates of analysis and traceability to national or international standards.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"6_Method_of_Analysis_Development_Procedure\"><\/span><strong>6. Method of Analysis Development Procedure<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<h3 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"61_Method_Development\"><\/span><strong>6.1. Method Development<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h3>\n\n\n\n<p>6.1.1 Define the objectives and requirements of the method, considering the packaging material type and regulatory guidelines.<\/p>\n\n\n\n<p>6.1.2 Select appropriate analytical techniques, such as spectroscopy, chromatography, or mechanical testing.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"62_Method_Validation\"><\/span><strong>6.2. Method Validation<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h3>\n\n\n\n<p>6.2.1 Validate the developed method by conducting validation studies, including specificity, linearity, accuracy, precision, and robustness.<\/p>\n\n\n\n<p>6.2.2 Document validation results and acceptance criteria.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"7_Documentation_and_Recordkeeping\"><\/span><strong>7. Documentation and Recordkeeping<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<h3 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"71_Method_Documentation\"><\/span><strong>7.1. Method Documentation<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h3>\n\n\n\n<p>7.1.1 Create a detailed method of analysis document, including method parameters, sample preparation, instrument settings, and calculations.<\/p>\n\n\n\n<p>7.1.2 Ensure that the method document is approved by the designated personnel.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"72_Method_Validation_Records\"><\/span><strong>7.2. Method Validation Records<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h3>\n\n\n\n<p>7.2.1 Maintain comprehensive records of method validation studies, including raw data, results, and any deviations or changes made during the validation process.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"8_Method_Revision_and_Review\"><\/span><strong>8. Method Revision and Review<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<h3 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"81_Revision_Process\"><\/span><strong>8.1. Revision Process<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h3>\n\n\n\n<p>8.1.1 Establish a process for the periodic review and revision of methods, ensuring that they remain up-to-date and compliant.<\/p>\n\n\n\n<p>8.1.2 Clearly define the responsibilities for method review and revision.<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>For more articles,&nbsp;<strong><a href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/ayurveda\/\">Kindly Click<\/a>&nbsp;here<\/strong>.<\/li>\n\n\n\n<li>For pharmaceutical jobs, follow us on<strong>&nbsp;<a href=\"https:\/\/www.linkedin.com\/company\/pharmaceuticalcarrier\/?viewAsMember=true\" target=\"_blank\" rel=\"noreferrer noopener\">LinkedIn<\/a><\/strong><\/li>\n\n\n\n<li><strong>For Editable SOPs in word format contact us on&nbsp;<a href=\"mailto:info@pharmaceuticalcarrier.com\">info@pharmaceuticalcarrier.com<\/a><\/strong><\/li>\n\n\n\n<li>For more information kindly follow us on pharmaguidelines.co.uk<\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>Explore a comprehensive Standard Operating Procedure (SOP) for the development and documentation of methods of analysis for packaging materials within [Company Name]. This SOP provides step-by-step guidance on method creation, validation, documentation, and revision, ensuring the quality control and compliance of packaging material analysis.<\/p>\n","protected":false},"author":1,"featured_media":5599,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_uag_custom_page_level_css":"","footnotes":""},"categories":[165],"tags":[751,270,677,285,750,749,735,257,276,166,752],"class_list":["post-5585","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-standard-operating-procedure","tag-analytical-techniques","tag-compliance","tag-laboratory-procedures","tag-method-development","tag-method-validation","tag-packaging-materials","tag-ppe","tag-quality-control","tag-safety-precautions","tag-sop","tag-writing-method-of-analysis-for-packaging-material"],"uagb_featured_image_src":{"full":["https:\/\/pharmaceuticalcarrier.com\/wp-content\/uploads\/2023\/09\/Standard-operating-procedure.jpg",1200,720,false],"thumbnail":["https:\/\/pharmaceuticalcarrier.com\/wp-content\/uploads\/2023\/09\/Standard-operating-procedure-150x150.jpg",150,150,true],"medium":["https:\/\/pharmaceuticalcarrier.com\/wp-content\/uploads\/2023\/09\/Standard-operating-procedure-300x180.jpg",300,180,true],"medium_large":["https:\/\/pharmaceuticalcarrier.com\/wp-content\/uploads\/2023\/09\/Standard-operating-procedure-768x461.jpg",640,384,true],"large":["https:\/\/pharmaceuticalcarrier.com\/wp-content\/uploads\/2023\/09\/Standard-operating-procedure-1024x614.jpg",640,384,true],"1536x1536":["https:\/\/pharmaceuticalcarrier.com\/wp-content\/uploads\/2023\/09\/Standard-operating-procedure.jpg",1200,720,false],"2048x2048":["https:\/\/pharmaceuticalcarrier.com\/wp-content\/uploads\/2023\/09\/Standard-operating-procedure.jpg",1200,720,false],"authorship-box-avatar":["https:\/\/pharmaceuticalcarrier.com\/wp-content\/uploads\/2023\/09\/Standard-operating-procedure-150x150.jpg",150,150,true],"authorship-box-related":["https:\/\/pharmaceuticalcarrier.com\/wp-content\/uploads\/2023\/09\/Standard-operating-procedure-70x70.jpg",70,70,true],"sow-carousel-default":["https:\/\/pharmaceuticalcarrier.com\/wp-content\/uploads\/2023\/09\/Standard-operating-procedure.jpg",272,163,false]},"uagb_author_info":{"display_name":"Pharmacareer","author_link":"https:\/\/pharmaceuticalcarrier.com\/index.php\/author\/grandirpharmagmail-com\/"},"uagb_comment_info":0,"uagb_excerpt":"Explore a comprehensive Standard Operating Procedure (SOP) for the development and documentation of methods of analysis for packaging materials within [Company Name]. This SOP provides step-by-step guidance on method creation, validation, documentation, and revision, ensuring the quality control and compliance of packaging material analysis.","amp_enabled":true,"_links":{"self":[{"href":"https:\/\/pharmaceuticalcarrier.com\/index.php\/wp-json\/wp\/v2\/posts\/5585","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/pharmaceuticalcarrier.com\/index.php\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/pharmaceuticalcarrier.com\/index.php\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/pharmaceuticalcarrier.com\/index.php\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/pharmaceuticalcarrier.com\/index.php\/wp-json\/wp\/v2\/comments?post=5585"}],"version-history":[{"count":1,"href":"https:\/\/pharmaceuticalcarrier.com\/index.php\/wp-json\/wp\/v2\/posts\/5585\/revisions"}],"predecessor-version":[{"id":5586,"href":"https:\/\/pharmaceuticalcarrier.com\/index.php\/wp-json\/wp\/v2\/posts\/5585\/revisions\/5586"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/pharmaceuticalcarrier.com\/index.php\/wp-json\/wp\/v2\/media\/5599"}],"wp:attachment":[{"href":"https:\/\/pharmaceuticalcarrier.com\/index.php\/wp-json\/wp\/v2\/media?parent=5585"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/pharmaceuticalcarrier.com\/index.php\/wp-json\/wp\/v2\/categories?post=5585"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/pharmaceuticalcarrier.com\/index.php\/wp-json\/wp\/v2\/tags?post=5585"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}