{"id":35211,"date":"2020-11-25T14:29:22","date_gmt":"2020-11-25T14:29:22","guid":{"rendered":"https:\/\/www.biotechpharmasummit.com\/?page_id=35211"},"modified":"2021-03-19T10:41:06","modified_gmt":"2021-03-19T10:41:06","slug":"julia-appelskog","status":"publish","type":"page","link":"https:\/\/www.biotechpharmasummit.com\/index.php\/pharmacovigilance-drug-safety-2021-speakers\/julia-appelskog\/","title":{"rendered":"Julia Appelskog"},"content":{"rendered":"<div class=\"vgblk-rw-wrapper limit-wrapper\">\n<h2>Julia Appelskog<\/h2>\n<h4>Pharmacovigilance Director, EU QPPV, Head of QPPVs &amp; Safety Consulting Services at TFS<\/h4>\n\t<p>Dr. Julia Appelskog is heading the EU QPPVs and Consulting Services at TFS, focusing on the strategic initiatives, innovation and integrated management system within PV. She about 20 years of experience in Pharmacovigilance combined with 8 years of experience in cancer and diabetes research.<\/p>\n<p>Julia was leading global teams as Head of PV QMS and Policy as well as Head of PV Strategy at Merck. For many years she was Head of Pharmacovigilance and EU QPPV and at Bluefish Pharmaceuticals. In previous roles at MSD, Johnson &amp; Johnson she was leading Nordic hubs and at Sanofi Pasteur MSD, besides Pharmacovigilance, she was also responsible for management of epidemiological and Clinical Trials, Quality Assurance, Regulatory Affairs and Medical Information.<\/p>\n<p>Dr. Appelskog has accomplished a PhD Thesis in cell biology and diabetes at the Karolinska Institute (Sweden) in 2001, followed by a postdoctoral fellow position at the Department of Clinical Neuroscience at Karolinska Institute, conducting research on epigenetic mechanisms, modification of DNA and its associated proteins in tumor cells.<\/p>\n<p>Julia is was an active member of EMA EudraVigilance Working Group (EWPWG), EuropaBio, International PV Working Group (IPWG) at EFPIA, &nbsp;TransCelerate, AESGP, Medicine for Europe and the Chairman of PV Working Group at Swedish Generic Medicines Association (FGL).<\/p>\n\t\t\t\t\t\t\t<img decoding=\"async\" loading=\"lazy\" src=\"https:\/\/www.biotechpharmasummit.com\/wp-content\/uploads\/2020\/11\/julia_appelskog_BioTech_Pharma_Summit_2021_Profile_1.jpg\" alt=\"julia_appelskog_BioTech_Pharma_Summit_2021_Profile_1\" itemprop=\"image\" height=\"1224\" width=\"820\" title=\"julia_appelskog_BioTech_Pharma_Summit_2021_Profile_1\" onerror=\"this.style.display='none'\" sizes=\"(max-width: 768px) 100vw, 100vw\" srcset=\"data:image\/svg+xml;utf8,<svg%20xmlns=&quot;http:\/\/www.w3.org\/2000\/svg&quot;%20viewBox=&quot;0%200%20820%201224&quot;%20height=&quot;1224px&quot;%20width=&quot;820px&quot;\/>&#8221; data-srcset=&#8221;https:\/\/www.biotechpharmasummit.com\/wp-content\/uploads\/2020\/11\/julia_appelskog_BioTech_Pharma_Summit_2021_Profile_1.jpg 820w, https:\/\/www.biotechpharmasummit.com\/wp-content\/uploads\/2020\/11\/julia_appelskog_BioTech_Pharma_Summit_2021_Profile_1-201&#215;300.jpg 201w, https:\/\/www.biotechpharmasummit.com\/wp-content\/uploads\/2020\/11\/julia_appelskog_BioTech_Pharma_Summit_2021_Profile_1-686&#215;1024.jpg 686w, https:\/\/www.biotechpharmasummit.com\/wp-content\/uploads\/2020\/11\/julia_appelskog_BioTech_Pharma_Summit_2021_Profile_1-768&#215;1146.jpg 768w, https:\/\/www.biotechpharmasummit.com\/wp-content\/uploads\/2020\/11\/julia_appelskog_BioTech_Pharma_Summit_2021_Profile_1-630&#215;940.jpg 630w, https:\/\/www.biotechpharmasummit.com\/wp-content\/uploads\/2020\/11\/julia_appelskog_BioTech_Pharma_Summit_2021_Profile_1-420&#215;627.jpg 420w, https:\/\/www.biotechpharmasummit.com\/wp-content\/uploads\/2020\/11\/julia_appelskog_BioTech_Pharma_Summit_2021_Profile_1-315&#215;470.jpg 315w&#8221;>\t\t\t\t\t\t\t\n<h3>\n\tTitle: How to define PV strategy and build an effective Regulatory Intelligence function \n\t<\/h3>\n\t<ul>\n<li>Strategy building methods<\/li>\n<li>Changes in PV regulations in 2020\/2021<\/li>\n<li>Staying ahead of regulatory changes<\/li>\n<\/ul>\n<h4>\n\t\t\t<a href=\"#\" title=\"On the Web\" target=\"_self\" rel=\"noopener noreferrer\">\n\tOn the Web\n\t\t\t<\/a>\n\t<\/h4>\n\t<p><a href=\"https:\/\/www.tfscro.com\/\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.tfscro.com\/<\/a><\/p>\n<h4>\n\t\t\t<a href=\"#\" title=\"On LinkedIn\" target=\"_self\" rel=\"noopener noreferrer\">\n\tOn LinkedIn\n\t\t\t<\/a>\n\t<\/h4>\n\t<p><a href=\"https:\/\/www.linkedin.com\/in\/julia-appelskog\/\" target=\"_blank\" rel=\"noopener noreferrer\">Visit Profile<\/a><\/p>\n<\/div><!-- .vgblk-rw-wrapper -->","protected":false},"excerpt":{"rendered":"<p>Julia Appelskog Pharmacovigilance Director, EU QPPV, Head of QPPVs &amp; Safety Consulting Services at TFS Dr. Julia Appelskog is heading the EU QPPVs and Consulting Services at TFS, focusing on the strategic initiatives, innovation and integrated management system within PV. She about 20 years of experience in Pharmacovigilance combined with 8 years of experience in&#8230;<\/p>\n","protected":false},"author":1,"featured_media":35212,"parent":35001,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"inline_featured_image":false,"footnotes":""},"class_list":["post-35211","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>Julia Appelskog &#8226; BioTech Pharma Summit<\/title>\n<meta name=\"description\" content=\"Dr. Julia Appelskog is heading the EU QPPVs and Consulting Services at TFS, focusing on the strategic initiatives, innovation and integrated management system within PV.\" \/>\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\/pharmacovigilance-drug-safety-2021-speakers\/julia-appelskog\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Julia Appelskog &#8226; 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