{"id":5115,"date":"2016-10-10T13:27:44","date_gmt":"2016-10-10T11:27:44","guid":{"rendered":"http:\/\/www.rapharm.eu\/en\/?p=5115"},"modified":"2016-11-23T17:35:06","modified_gmt":"2016-11-23T16:35:06","slug":"cycles-of-regular-pharmaceutical-regulatory-seminars-autumn-2016-and-spring-2017","status":"publish","type":"post","link":"https:\/\/www.rapharm.eu\/en\/cycles-of-regular-pharmaceutical-regulatory-seminars-autumn-2016-and-spring-2017\/","title":{"rendered":"Cycles of regular pharmaceutical regulatory seminars AUTUMN 2016 and SPRING 2017"},"content":{"rendered":"<style type=\"text\/css\"><\/style><p><strong>Cycles of regular pharmaceutical regulatory seminars AUTUMN 2016 and SPRING 2017<\/strong><br \/>\n<strong>Radisson Blu Plaza Hotel\u00a0Ljubljana\u00a0(Slovenian language)<\/strong><\/p>\n<p>In the cycles of regular pharmaceutical regulatory seminars Autumn 2016 and Spring 2017 we have prepared a comprehensive education in the field of pharmaceutical regulatory affairs. The education offers understanding and managing of the regulatory affairs of medicinal products as a whole and as well a deepening into specific areas. This time, Cycles will be organised as ten individual seminar, five in the autumn and five in the spring series.<\/p>\n<p>Education is intended for assosiates in the pharmaceutical industry working in different areas, from medicinal products developement to regulatory departments and marketing, for assosiates in competent authorities and others who need the aforementioned skills. Specialised skills do not suffice to make suitable decisions\u00a0in practice,\u00a0one needs to understand the whole and as well the\u00a0consequences of decisions. As this is one of the most regulatad areas in the EU legislation, it is in order to occasionally refresh the existing knowledge, as a precondition for highly professional task performance in this field.<\/p>\n<p>Seminars are run by<strong>\u00a0Vesna Koblar, MD. PhD. with guests<\/strong>, experts in certain areas.<\/p>\n<p>&nbsp;<\/p>\n<p><strong>AUTUMN\u00a02016<\/strong><\/p>\n<p>Seminar 1<br \/>\n<strong>INTRODUCTION TO EU PHARMACEUTICAL REGULATORY ACQUIS AND HOW TO ACHIEVE ITS GOALS: HIGH LEVEL OF PUBLIC PROTECTION AND COMPETITIVENESS OF PHARMACEUTICAL INDUSTRY<\/strong><br \/>\n5th December 2016, 14 h \u2013 17 h<\/p>\n<p>Seminar 2<br \/>\n<strong>MARKETING AUTHORISATION PROCEDURES AND DOCUMENTATION, SPECIFIC REQUIREMENTS<br \/>\n<\/strong>6th December 2016, 14 h \u2013 17 h<\/p>\n<p>Seminar 3<strong><br \/>\n<\/strong><strong>VARIATIONS TO MARKETING AUTHORISATION AND EXTENSION LINES<br \/>\n<\/strong>7th December 2016, 14 h \u2013 17 h<\/p>\n<p>Seminar 4<strong><br \/>\n<\/strong><strong>TYPES OF APPLICATION FOR MARKETING AUTHORISATION; CHOICES, REQUIREMENTS, STRATEGIC USE IN PRACTICE, THE MOST COMMON ERRORS<br \/>\n<\/strong>8th December 2016, 14 h \u2013 17 h<\/p>\n<p>Seminar 5<strong><br \/>\n<\/strong><strong>REGULATORY SPECIFICS OF BIOLOGICAL MEDICINAL PRODUCTS AND ADVANCED THERAPY MEDICINAL PRODUCTS<br \/>\n<\/strong>9th December 2016, 14 h \u2013 17 h<\/p>\n<p>&nbsp;<\/p>\n<p><strong>SPRING\u00a02017<\/strong><\/p>\n<p>Seminar 6<strong><br \/>\n<\/strong><strong>PHARMACOVIGILANCE<br \/>\n<\/strong>3rd April 2017, 14 h \u2013 17 h<\/p>\n<p>Seminar 7<strong><br \/>\n<\/strong><strong>CLINICAL INVESTIGATION OF MEDICINAL PRODUCTS<br \/>\n<\/strong>4th April 2017, 14 h \u2013 17 h<\/p>\n<p>Seminar 8<strong><br \/>\n<\/strong><strong>ADVERTISING AND INFORMING ON MEDICINAL PRODUCTS<br \/>\n<\/strong>5th April 2017, 14 h \u2013 17 h<\/p>\n<p>Seminar 9<strong><br \/>\n<\/strong><strong>BORDERLINE PRODUCTS IN THE PHARMACEUTICAL INDUSTRY<br \/>\n<\/strong>6th April 2017, 14 h \u2013 17 h<\/p>\n<p>Seminar 10<strong><br \/>\n<\/strong><strong>COMBINATION PRODUCTS: MEDICINAL PRODUCT &#8211; MEDICAL DEVICE AND NEW REGULATIONS<br \/>\n<\/strong>7th April 2017, 14 h \u2013 17 h<\/p>\n<p>&nbsp;<\/p>\n<p>Click <a href=\"http:\/\/www.rapharm.eu\/wp-content\/uploads\/2016\/10\/raPHARM_Jesen2016Pomlad2017-1.pdf\" target=\"_blank\">HERE<\/a> for more information.<\/p>\n<p>Click <a href=\"http:\/\/www.rapharm.eu\/en\/application-form\/\" target=\"_blank\">HERE<\/a> to apply for seminars.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Cycles of regular pharmaceutical regulatory seminars AUTUMN 2016 and SPRING 2017 Radisson Blu Plaza Hotel\u00a0Ljubljana\u00a0(Slovenian language) In the cycles of regular pharmaceutical regulatory seminars Autumn 2016 and Spring 2017 we have prepared a comprehensive education in the field of pharmaceutical regulatory affairs. The education offers understanding and managing of the regulatory affairs of medicinal products&#8230;<\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[40,39],"tags":[],"class_list":["post-5115","post","type-post","status-publish","format-standard","hentry","category-current-educations-and-trainings","category-regulatory-news"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v25.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Cycles of regular pharmaceutical regulatory seminars AUTUMN 2016 and SPRING 2017 - raPHARM<\/title>\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.rapharm.eu\/ciklusa-rednih-farmacevtskih-regulatornih-seminarjev-jesen-2016-in-pomlad-2017\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Cycles of regular pharmaceutical regulatory seminars AUTUMN 2016 and SPRING 2017 - raPHARM\" \/>\n<meta property=\"og:description\" content=\"Cycles of regular pharmaceutical regulatory seminars AUTUMN 2016 and SPRING 2017 Radisson Blu Plaza Hotel\u00a0Ljubljana\u00a0(Slovenian language) In the cycles of regular pharmaceutical regulatory seminars Autumn 2016 and Spring 2017 we have prepared a comprehensive education in the field of pharmaceutical regulatory affairs. 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