{"id":33529,"date":"2020-08-13T15:09:00","date_gmt":"2020-08-13T14:09:00","guid":{"rendered":"https:\/\/www.biotechpharmasummit.com\/?page_id=33529"},"modified":"2023-05-02T22:21:29","modified_gmt":"2023-05-02T21:21:29","slug":"steinar-madsen","status":"publish","type":"page","link":"https:\/\/www.biotechpharmasummit.com\/index.php\/biosimilars-biologics-2019-speakers\/steinar-madsen\/","title":{"rendered":"Steinar Madsen"},"content":{"rendered":"<div class=\"vgblk-rw-wrapper limit-wrapper\">\n\n\t<h2>Steinar Madsen<\/h2>\n<h4>Medical Director at Norwegian Medicines Agency<\/h4>\n\t<p>Dr. Steinar Madsen is medical director at the Norwegian Medicines Agency. He has been working with generic substitution since it was introduced in Norway in 2001 and with biosimilars since 2006. He is member and previously chairman of the committee for generic substitution at the Agency. Dr. Madsen is also engaged in the drug information service, with a special interest in the safe and cost-effective use of drugs. He is a specialist in internal medicine and cardiology and works part time as a consultant in cardiology.<\/p>\n\t\t\t\t\t\t\t<img decoding=\"async\" loading=\"lazy\" src=\"https:\/\/www.biotechpharmasummit.com\/wp-content\/uploads\/2020\/07\/Steinar_Madsen_BioTech_Pharma_Summit_Norwegian_medicine_agency_profile.jpg\" alt=\"Steinar_Madsen_BioTech_Pharma_Summit_Norwegian_medicine_agency_profile\" itemprop=\"image\" height=\"1224\" width=\"820\" title=\"Steinar_Madsen_BioTech_Pharma_Summit_Norwegian_medicine_agency_profile\" onerror=\"this.style.display='none'\"  sizes=\"auto, (max-width: 768px) 100vw, 100vw\" srcset=\"https:\/\/www.biotechpharmasummit.com\/wp-content\/uploads\/2020\/07\/Steinar_Madsen_BioTech_Pharma_Summit_Norwegian_medicine_agency_profile.jpg 820w, https:\/\/www.biotechpharmasummit.com\/wp-content\/uploads\/2020\/07\/Steinar_Madsen_BioTech_Pharma_Summit_Norwegian_medicine_agency_profile-201x300.jpg 201w, https:\/\/www.biotechpharmasummit.com\/wp-content\/uploads\/2020\/07\/Steinar_Madsen_BioTech_Pharma_Summit_Norwegian_medicine_agency_profile-686x1024.jpg 686w, https:\/\/www.biotechpharmasummit.com\/wp-content\/uploads\/2020\/07\/Steinar_Madsen_BioTech_Pharma_Summit_Norwegian_medicine_agency_profile-768x1146.jpg 768w, https:\/\/www.biotechpharmasummit.com\/wp-content\/uploads\/2020\/07\/Steinar_Madsen_BioTech_Pharma_Summit_Norwegian_medicine_agency_profile-630x940.jpg 630w, https:\/\/www.biotechpharmasummit.com\/wp-content\/uploads\/2020\/07\/Steinar_Madsen_BioTech_Pharma_Summit_Norwegian_medicine_agency_profile-420x627.jpg 420w, https:\/\/www.biotechpharmasummit.com\/wp-content\/uploads\/2020\/07\/Steinar_Madsen_BioTech_Pharma_Summit_Norwegian_medicine_agency_profile-315x470.jpg 315w\" \/>\t\t\t\t\t\t\t\n<h3>\n\tTitle: Biosimlars are accepted &#8211; but is it sustainable?\n\t<\/h3>\n\t<a href=\"https:\/\/sociopharma.com\/\" target=\"_blank\" role=\"button\" rel=\"noopener\">\n\t\t\t\t\tPresentation available only at SocioPharma.com\n\t<\/a>\n<h4>\n\t\t\t<a href=\"#\" title=\"On the Web\" target=\"_self\" rel=\"noopener\">\n\tOn the Web\n\t\t\t<\/a>\n\t<\/h4>\n\t<p><a href=\"https:\/\/legemiddelverket.no\/english\" target=\"_blank\" rel=\"noopener\">https:\/\/legemiddelverket.no\/english<\/a><\/p>\n<h4>\n\t\t\t<a href=\"#\" title=\"On LinkedIn\" target=\"_self\" rel=\"noopener\">\n\tOn LinkedIn\n\t\t\t<\/a>\n\t<\/h4>\n\t<p><a href=\"https:\/\/www.linkedin.com\/in\/steinar-madsen-6aa448a1\/\" target=\"_blank\" rel=\"noopener\">Visit Profile<\/a><\/p>\n\n<\/div><!-- .vgblk-rw-wrapper -->","protected":false},"excerpt":{"rendered":"<p>Steinar Madsen Medical Director at Norwegian Medicines Agency Dr. Steinar Madsen is medical director at the Norwegian Medicines Agency. He has been working with generic substitution since it was introduced in Norway in 2001 and with biosimilars since 2006. He is member and previously chairman of the committee for generic substitution at the Agency. Dr&#8230;.<\/p>\n","protected":false},"author":1,"featured_media":32397,"parent":33455,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"inline_featured_image":false,"footnotes":""},"class_list":["post-33529","page","type-page","status-publish","has-post-thumbnail","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.2 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Steinar Madsen &#8226; BioTech Pharma Summit<\/title>\n<meta name=\"description\" content=\"Dr. Steinar Madsen is medical director at the Norwegian Medicines Agency. He has been working with generic substitution since it was introduced in Norway in 2001\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.biotechpharmasummit.com\/index.php\/biosimilars-biologics-2019-speakers\/steinar-madsen\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Steinar Madsen &#8226; BioTech Pharma Summit\" \/>\n<meta property=\"og:description\" content=\"Dr. Steinar Madsen is medical director at the Norwegian Medicines Agency. 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