{"id":5949,"date":"2022-09-30T15:30:00","date_gmt":"2022-09-30T13:30:00","guid":{"rendered":"https:\/\/m2apartners.cz\/mdr-for-the-fourth-time-technical-documentation\/"},"modified":"2025-03-27T17:04:57","modified_gmt":"2025-03-27T16:04:57","slug":"mdr-for-the-fourth-time-technical-documentation","status":"publish","type":"post","link":"https:\/\/m2apartners.cz\/en\/mdr-for-the-fourth-time-technical-documentation\/","title":{"rendered":"MDR for the fourth time – technical documentation"},"content":{"rendered":"\n

In our fourth article, we will focus on the technical documentation that manufacturers of medical devices are obliged to prepare and keep up-to-date for their products according to the new regulation. The full article is available here: https:\/\/www.tribune.cz\/clanek\/44735-mdr-poctvrte-technicka-dokumentace<\/a> <\/p>\n","protected":false},"excerpt":{"rendered":"

In our fourth article, we will focus on the technical documentation that manufacturers of medical devices are obliged to prepare and keep up-to-date for their products according to the new regulation. The full article is available here: https:\/\/www.tribune.cz\/clanek\/44735-mdr-poctvrte-technicka-dokumentace<\/p>\n","protected":false},"author":1,"featured_media":5525,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_et_pb_use_builder":"","_et_pb_old_content":"","_et_gb_content_width":"","inline_featured_image":false,"footnotes":""},"categories":[320,357],"tags":[358,360,511],"class_list":["post-5949","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-articles","category-medical-devices","tag-eu-legislation","tag-mdr-en","tag-pharmaceutical-industry"],"yoast_head":"\nMDR for the fourth time - technical documentation - m2apartners.cz<\/title>\n<meta name=\"description\" content=\"In our fourth article, we will focus on the technical documentation that manufacturers of medical devices are obliged to prepare and keep up-to-date for their products according to the new regulation. The full article is available here: https:\/\/www.tribune.cz\/clanek\/44735-mdr-poctvrte-technicka-dokumentace\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/m2apartners.cz\/en\/mdr-for-the-fourth-time-technical-documentation\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"MDR for the fourth time - technical documentation - m2apartners.cz\" \/>\n<meta property=\"og:description\" content=\"In our fourth article, we will focus on the technical documentation that manufacturers of medical devices are obliged to prepare and keep up-to-date for their products according to the new regulation. The full article is available here: https:\/\/www.tribune.cz\/clanek\/44735-mdr-poctvrte-technicka-dokumentace\" \/>\n<meta property=\"og:url\" content=\"https:\/\/m2apartners.cz\/en\/mdr-for-the-fourth-time-technical-documentation\/\" \/>\n<meta property=\"og:site_name\" content=\"m2apartners.cz\" \/>\n<meta property=\"article:published_time\" content=\"2022-09-30T13:30:00+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2025-03-27T16:04:57+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/m2apartners.cz\/wp-content\/uploads\/2022\/09\/4.png\" \/>\n\t<meta property=\"og:image:width\" content=\"940\" \/>\n\t<meta property=\"og:image:height\" content=\"788\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/png\" \/>\n<meta name=\"author\" content=\"admin3645\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"admin3645\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/mdr-for-the-fourth-time-technical-documentation\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/mdr-for-the-fourth-time-technical-documentation\\\/\"},\"author\":{\"name\":\"admin3645\",\"@id\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/#\\\/schema\\\/person\\\/2737d6d592b954976f2a3fdcb4e8248e\"},\"headline\":\"MDR for the fourth time – technical documentation\",\"datePublished\":\"2022-09-30T13:30:00+00:00\",\"dateModified\":\"2025-03-27T16:04:57+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/mdr-for-the-fourth-time-technical-documentation\\\/\"},\"wordCount\":51,\"publisher\":{\"@id\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/#organization\"},\"image\":{\"@id\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/mdr-for-the-fourth-time-technical-documentation\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/m2apartners.cz\\\/wp-content\\\/uploads\\\/2022\\\/09\\\/4.png\",\"keywords\":[\"EU legislation\",\"MDR\",\"pharmaceutical industry\"],\"articleSection\":[\"Articles\",\"Medical devices\"],\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/mdr-for-the-fourth-time-technical-documentation\\\/\",\"url\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/mdr-for-the-fourth-time-technical-documentation\\\/\",\"name\":\"MDR for the fourth time - technical documentation - m2apartners.cz\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/#website\"},\"primaryImageOfPage\":{\"@id\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/mdr-for-the-fourth-time-technical-documentation\\\/#primaryimage\"},\"image\":{\"@id\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/mdr-for-the-fourth-time-technical-documentation\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/m2apartners.cz\\\/wp-content\\\/uploads\\\/2022\\\/09\\\/4.png\",\"datePublished\":\"2022-09-30T13:30:00+00:00\",\"dateModified\":\"2025-03-27T16:04:57+00:00\",\"description\":\"In our fourth article, we will focus on the technical documentation that manufacturers of medical devices are obliged to prepare and keep up-to-date for their products according to the new regulation. The full article is available here: https:\\\/\\\/www.tribune.cz\\\/clanek\\\/44735-mdr-poctvrte-technicka-dokumentace\",\"breadcrumb\":{\"@id\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/mdr-for-the-fourth-time-technical-documentation\\\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\\\/\\\/m2apartners.cz\\\/en\\\/mdr-for-the-fourth-time-technical-documentation\\\/\"]}]},{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/mdr-for-the-fourth-time-technical-documentation\\\/#primaryimage\",\"url\":\"https:\\\/\\\/m2apartners.cz\\\/wp-content\\\/uploads\\\/2022\\\/09\\\/4.png\",\"contentUrl\":\"https:\\\/\\\/m2apartners.cz\\\/wp-content\\\/uploads\\\/2022\\\/09\\\/4.png\",\"width\":940,\"height\":788,\"caption\":\"Technick\u00e1 dokumentace\"},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/mdr-for-the-fourth-time-technical-documentation\\\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"MDR for the fourth time - technical documentation\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/#website\",\"url\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/\",\"name\":\"m2apartners.cz\",\"description\":\"We focus on providing legal services to clients in the pharmaceutical and medical device industries, in corporate matters, in connection with the setting up of internal processes, in matters of zoning and construction law proceedings, in general practice, especially general contract, real estate, family and employment law.\",\"publisher\":{\"@id\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/#organization\"},\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"},{\"@type\":\"Organization\",\"@id\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/#organization\",\"name\":\"M2A Partners\",\"url\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/\",\"logo\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/#\\\/schema\\\/logo\\\/image\\\/\",\"url\":\"https:\\\/\\\/m2apartners.cz\\\/wp-content\\\/uploads\\\/2025\\\/03\\\/cropped-cropped-FAV_512x512.png\",\"contentUrl\":\"https:\\\/\\\/m2apartners.cz\\\/wp-content\\\/uploads\\\/2025\\\/03\\\/cropped-cropped-FAV_512x512.png\",\"width\":512,\"height\":512,\"caption\":\"M2A Partners\"},\"image\":{\"@id\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/#\\\/schema\\\/logo\\\/image\\\/\"}},{\"@type\":\"Person\",\"@id\":\"https:\\\/\\\/m2apartners.cz\\\/en\\\/#\\\/schema\\\/person\\\/2737d6d592b954976f2a3fdcb4e8248e\",\"name\":\"admin3645\",\"image\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\\\/\\\/secure.gravatar.com\\\/avatar\\\/baf40bb2dd82590384e4496ea9a16e5723a6284ec7fb445ad629f19905b6c337?s=96&d=mm&r=g\",\"url\":\"https:\\\/\\\/secure.gravatar.com\\\/avatar\\\/baf40bb2dd82590384e4496ea9a16e5723a6284ec7fb445ad629f19905b6c337?s=96&d=mm&r=g\",\"contentUrl\":\"https:\\\/\\\/secure.gravatar.com\\\/avatar\\\/baf40bb2dd82590384e4496ea9a16e5723a6284ec7fb445ad629f19905b6c337?s=96&d=mm&r=g\",\"caption\":\"admin3645\"},\"sameAs\":[\"https:\\\/\\\/m2apartners.cz\"]}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"MDR for the fourth time - technical documentation - m2apartners.cz","description":"In our fourth article, we will focus on the technical documentation that manufacturers of medical devices are obliged to prepare and keep up-to-date for their products according to the new regulation. The full article is available here: https:\/\/www.tribune.cz\/clanek\/44735-mdr-poctvrte-technicka-dokumentace","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/m2apartners.cz\/en\/mdr-for-the-fourth-time-technical-documentation\/","og_locale":"en_US","og_type":"article","og_title":"MDR for the fourth time - technical documentation - m2apartners.cz","og_description":"In our fourth article, we will focus on the technical documentation that manufacturers of medical devices are obliged to prepare and keep up-to-date for their products according to the new regulation. The full article is available here: https:\/\/www.tribune.cz\/clanek\/44735-mdr-poctvrte-technicka-dokumentace","og_url":"https:\/\/m2apartners.cz\/en\/mdr-for-the-fourth-time-technical-documentation\/","og_site_name":"m2apartners.cz","article_published_time":"2022-09-30T13:30:00+00:00","article_modified_time":"2025-03-27T16:04:57+00:00","og_image":[{"width":940,"height":788,"url":"https:\/\/m2apartners.cz\/wp-content\/uploads\/2022\/09\/4.png","type":"image\/png"}],"author":"admin3645","twitter_card":"summary_large_image","twitter_misc":{"Written by":"admin3645"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/m2apartners.cz\/en\/mdr-for-the-fourth-time-technical-documentation\/#article","isPartOf":{"@id":"https:\/\/m2apartners.cz\/en\/mdr-for-the-fourth-time-technical-documentation\/"},"author":{"name":"admin3645","@id":"https:\/\/m2apartners.cz\/en\/#\/schema\/person\/2737d6d592b954976f2a3fdcb4e8248e"},"headline":"MDR for the fourth time – technical documentation","datePublished":"2022-09-30T13:30:00+00:00","dateModified":"2025-03-27T16:04:57+00:00","mainEntityOfPage":{"@id":"https:\/\/m2apartners.cz\/en\/mdr-for-the-fourth-time-technical-documentation\/"},"wordCount":51,"publisher":{"@id":"https:\/\/m2apartners.cz\/en\/#organization"},"image":{"@id":"https:\/\/m2apartners.cz\/en\/mdr-for-the-fourth-time-technical-documentation\/#primaryimage"},"thumbnailUrl":"https:\/\/m2apartners.cz\/wp-content\/uploads\/2022\/09\/4.png","keywords":["EU legislation","MDR","pharmaceutical industry"],"articleSection":["Articles","Medical devices"],"inLanguage":"en-US"},{"@type":"WebPage","@id":"https:\/\/m2apartners.cz\/en\/mdr-for-the-fourth-time-technical-documentation\/","url":"https:\/\/m2apartners.cz\/en\/mdr-for-the-fourth-time-technical-documentation\/","name":"MDR for the fourth time - technical documentation - m2apartners.cz","isPartOf":{"@id":"https:\/\/m2apartners.cz\/en\/#website"},"primaryImageOfPage":{"@id":"https:\/\/m2apartners.cz\/en\/mdr-for-the-fourth-time-technical-documentation\/#primaryimage"},"image":{"@id":"https:\/\/m2apartners.cz\/en\/mdr-for-the-fourth-time-technical-documentation\/#primaryimage"},"thumbnailUrl":"https:\/\/m2apartners.cz\/wp-content\/uploads\/2022\/09\/4.png","datePublished":"2022-09-30T13:30:00+00:00","dateModified":"2025-03-27T16:04:57+00:00","description":"In our fourth article, we will focus on the technical documentation that manufacturers of medical devices are obliged to prepare and keep up-to-date for their products according to the new regulation. The full article is available here: https:\/\/www.tribune.cz\/clanek\/44735-mdr-poctvrte-technicka-dokumentace","breadcrumb":{"@id":"https:\/\/m2apartners.cz\/en\/mdr-for-the-fourth-time-technical-documentation\/#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/m2apartners.cz\/en\/mdr-for-the-fourth-time-technical-documentation\/"]}]},{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/m2apartners.cz\/en\/mdr-for-the-fourth-time-technical-documentation\/#primaryimage","url":"https:\/\/m2apartners.cz\/wp-content\/uploads\/2022\/09\/4.png","contentUrl":"https:\/\/m2apartners.cz\/wp-content\/uploads\/2022\/09\/4.png","width":940,"height":788,"caption":"Technick\u00e1 dokumentace"},{"@type":"BreadcrumbList","@id":"https:\/\/m2apartners.cz\/en\/mdr-for-the-fourth-time-technical-documentation\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/m2apartners.cz\/en\/"},{"@type":"ListItem","position":2,"name":"MDR for the fourth time - technical documentation"}]},{"@type":"WebSite","@id":"https:\/\/m2apartners.cz\/en\/#website","url":"https:\/\/m2apartners.cz\/en\/","name":"m2apartners.cz","description":"We focus on providing legal services to clients in the pharmaceutical and medical device industries, in corporate matters, in connection with the setting up of internal processes, in matters of zoning and construction law proceedings, in general practice, especially general contract, real estate, family and employment law.","publisher":{"@id":"https:\/\/m2apartners.cz\/en\/#organization"},"potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/m2apartners.cz\/en\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"en-US"},{"@type":"Organization","@id":"https:\/\/m2apartners.cz\/en\/#organization","name":"M2A Partners","url":"https:\/\/m2apartners.cz\/en\/","logo":{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/m2apartners.cz\/en\/#\/schema\/logo\/image\/","url":"https:\/\/m2apartners.cz\/wp-content\/uploads\/2025\/03\/cropped-cropped-FAV_512x512.png","contentUrl":"https:\/\/m2apartners.cz\/wp-content\/uploads\/2025\/03\/cropped-cropped-FAV_512x512.png","width":512,"height":512,"caption":"M2A Partners"},"image":{"@id":"https:\/\/m2apartners.cz\/en\/#\/schema\/logo\/image\/"}},{"@type":"Person","@id":"https:\/\/m2apartners.cz\/en\/#\/schema\/person\/2737d6d592b954976f2a3fdcb4e8248e","name":"admin3645","image":{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/secure.gravatar.com\/avatar\/baf40bb2dd82590384e4496ea9a16e5723a6284ec7fb445ad629f19905b6c337?s=96&d=mm&r=g","url":"https:\/\/secure.gravatar.com\/avatar\/baf40bb2dd82590384e4496ea9a16e5723a6284ec7fb445ad629f19905b6c337?s=96&d=mm&r=g","contentUrl":"https:\/\/secure.gravatar.com\/avatar\/baf40bb2dd82590384e4496ea9a16e5723a6284ec7fb445ad629f19905b6c337?s=96&d=mm&r=g","caption":"admin3645"},"sameAs":["https:\/\/m2apartners.cz"]}]}},"_links":{"self":[{"href":"https:\/\/m2apartners.cz\/en\/wp-json\/wp\/v2\/posts\/5949","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/m2apartners.cz\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/m2apartners.cz\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/m2apartners.cz\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/m2apartners.cz\/en\/wp-json\/wp\/v2\/comments?post=5949"}],"version-history":[{"count":1,"href":"https:\/\/m2apartners.cz\/en\/wp-json\/wp\/v2\/posts\/5949\/revisions"}],"predecessor-version":[{"id":5951,"href":"https:\/\/m2apartners.cz\/en\/wp-json\/wp\/v2\/posts\/5949\/revisions\/5951"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/m2apartners.cz\/en\/wp-json\/wp\/v2\/media\/5525"}],"wp:attachment":[{"href":"https:\/\/m2apartners.cz\/en\/wp-json\/wp\/v2\/media?parent=5949"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/m2apartners.cz\/en\/wp-json\/wp\/v2\/categories?post=5949"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/m2apartners.cz\/en\/wp-json\/wp\/v2\/tags?post=5949"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}