{"id":55626,"date":"2023-04-10T11:03:21","date_gmt":"2023-04-10T09:03:21","guid":{"rendered":"https:\/\/pharma-trend.com\/en\/final-weeks-to-register-2-day-pharmaceutical-regulatory-affairs-in-asia-training-course-all-important-aspects-of-gaining-and-maintaining-a-successful-marketing-authorisation-june-14-16-2023-re\/"},"modified":"2023-04-10T11:03:21","modified_gmt":"2023-04-10T09:03:21","slug":"final-weeks-to-register-2-day-pharmaceutical-regulatory-affairs-in-asia-training-course-all-important-aspects-of-gaining-and-maintaining-a-successful-marketing-authorisation-june-14-16-2023-re","status":"publish","type":"post","link":"https:\/\/pharma-trend.com\/en\/final-weeks-to-register-2-day-pharmaceutical-regulatory-affairs-in-asia-training-course-all-important-aspects-of-gaining-and-maintaining-a-successful-marketing-authorisation-june-14-16-2023-re\/","title":{"rendered":"Final Weeks to Register: 2 Day Pharmaceutical Regulatory Affairs in Asia Training Course &#8211; All Important Aspects of Gaining and Maintaining a Successful Marketing Authorisation (June 14-16, 2023) &#8211; ResearchAndMarkets.com"},"content":{"rendered":"<div>\n<p>DUBLIN&#8211;(BUSINESS WIRE)&#8211;The <a target=\"_blank\" href=\"https:\/\/www.researchandmarkets.com\/reports\/5725561\/pharmaceutical-regulatory-affairs-in-asia?utm_source=BW&amp;utm_medium=PressRelease&amp;utm_code=v2pwpt&amp;utm_campaign=1816161+-+Final+Weeks+to+Register%3A+2+Day+Pharmaceutical+Regulatory+Affairs+in+Asia+Training+Course+-+All+Important+Aspects+of+Gaining+and+Maintaining+a+Successful+Marketing+Authorisation+(June+14-16%2C+2023)&amp;utm_exec=chdo54prd\" rel=\"nofollow noopener\" shape=\"rect\">&#8220;Pharmaceutical Regulatory Affairs in Asia Training Course&#8221;<\/a> conference has been added to <strong>ResearchAndMarkets.com&#8217;s<\/strong> offering.<\/p>\n<p><a href=\"https:\/\/mms.businesswire.com\/media\/20230410005160\/en\/1759349\/4\/logo.jpg\"><img decoding=\"async\" src=\"https:\/\/mms.businesswire.com\/media\/20230410005160\/en\/1759349\/21\/logo.jpg\"><\/a><\/p>\n<p>\nThis seminar will provide a practical overview of the key areas of pharmaceutical regulatory affairs in Asia, including India, and will cover all important aspects of gaining and maintaining a successful marketing authorisation within the region.<\/p>\n<p>\nThe pharmaceutical market in Asia is growing at a rapid pace and presents both opportunities and challenges to those wishing to work in the region. Rather than a single market, Asia is a collection of different markets, each with their own regulatory processes, although harmonisation exists within the ASEAN countries.<\/p>\n<p>\n<strong>The programme will include:<\/strong><\/p>\n<ul>\n<li>\nDiscussion of underlying official regulatory sources<\/li>\n<li>\nAn interpretation of practical aspects<\/li>\n<li>\nAn overview of the requirements for local manufacturing<\/li>\n<li>\nRecent developments<\/li>\n<li>\nHarmonisation initiatives<\/li>\n<li>\nAn update and wider knowledge of regulatory affairs in Asia<\/li>\n<li>\nThe opportunity to exchange experiences with other delegates<\/li>\n<\/ul>\n<p>\n<strong>Benefits of attending:<\/strong><\/p>\n<ul>\n<li>\nGain an overview of key Asian markets<\/li>\n<li>\nDiscuss outlines of company and product registration<\/li>\n<li>\nUnderstand the application process<\/li>\n<li>\nAssess the impact of recent regulatory developments in the region<\/li>\n<li>\nDiscuss harmonisation initiatives including ASEAN opportunities<\/li>\n<li>\nUnderstand how Japan fits in the Asian regulatory landscape<\/li>\n<li>\nDiscover general, country-specific and regional requirements<\/li>\n<\/ul>\n<p>\nPlease note that the course will provide an excellent introduction to all the key aspects of regulatory affairs in the Asia region but will not focus specifically or in detail on Chemistry, Manufacture and Control (CMC).<\/p>\n<p>\n<strong>Who Should Attend:<\/strong><\/p>\n<p>\nThis seminar will be of particular interest to all those who need to learn about successful marketing authorisation applications and in-market regulatory compliance, whether as an introductory or a refresher course.<\/p>\n<p>\n<strong>Previous delegates have included:<\/strong><\/p>\n<ul>\n<li>\nScientists and technical staff in<\/p>\n<ul>\n<li>\nRegulatory affairs<\/li>\n<li>\nRegistration departments<\/li>\n<\/ul>\n<\/li>\n<li>\nMedical directors<\/li>\n<\/ul>\n<p>\n<strong>Key Topics Covered:<\/strong><\/p>\n<ul>\n<li>\nIntroduction to the Asia Region<\/li>\n<li>\nIntroduction to ASEAN<\/li>\n<li>\nPhilippines<\/li>\n<li>\nBrunei<\/li>\n<li>\nPR of China<\/li>\n<li>\nIndia<\/li>\n<li>\nMalaysia<\/li>\n<li>\nSingapore<\/li>\n<li>\nHong Kong<\/li>\n<li>\nIndonesia<\/li>\n<li>\nThailand<\/li>\n<li>\nVietnam\/Cambodia\/Laos<\/li>\n<li>\nTaiwan<\/li>\n<li>\nKorea<\/li>\n<li>\nOutline on Japan<\/li>\n<li>\nAsean Harmonisation<\/li>\n<\/ul>\n<p>\n<strong>Speakers:<\/strong><\/p>\n<p>\n<strong>Monica Dressler-Meyer<\/strong><\/p>\n<p>\nDRA Manager<\/p>\n<p>\nManagement Forum<\/p>\n<p>\nM\u00f3nica is DRA Manager based in Switzerland with several years of regulatory experience. She has spent many years in DRA working with different pharmaceutical companies with responsibility for Asia Pacific and lately also for development activities in other regions. Prior to this, she worked at F. Hoffmann-La Roche in Switzerland where she gained several years&#8217; experience in industry basics and pre-clinical research. M\u00f3nica has a Degree in Chemistry and Biochemistry from Basel University.<\/p>\n<p>\n<strong>Alan Chalmers<\/strong><\/p>\n<p>\nPharmacist<\/p>\n<p>\nManagement Forum<\/p>\n<p>\nDr Alan Chalmers is a pharmacist with over 35 industrial experiences mainly in the field of pharmaceutical regulatory affairs. A graduate of Strathclyde University in Glasgow with a B.Sc. in Pharmacy with specialisation in Pharmaceutical Technology, his Ph.D. at Manchester University was in Pharmaceutical Formulation. From 1975-1978 he was Development Officer and Clinical Trials Pharmacist of Allen &amp; Hanburys (part of the then Glaxo group). In 1978 he joined Ciba-Geigy in DRA. Over 20 years were spent with Ciba-Geigy\/CIBA\/Novartis in all aspects of regulatory affairs including head of a group company DRA in Canada and for many years as Head of Pharma International regulatory affairs.<\/p>\n<p>\nHe has been consultant to the IFPMA, WHO and other international bodies and was Chairman of the Organising Committee of the initial IFPMA Asian Regulatory Conferences in Hong Kong and Singapore and Rapporteur to the more recent conferences in China and Malaysia.<\/p>\n<p>\nSince 1998 he has been an independent regulatory consultant and is Director of his own consultancy company Pharma International in Switzerland. He has also been director of two UK and Swiss registered pharmaceutical companies with specialised responsibility for international regulatory strategy. More recently as accredited by Swissmedic, Dr. Chalmers is a Qualified Person supporting several Swiss pharmaceutical companies trading internationally with pharmaceuticals and medical devices.<\/p>\n<p>\nHe is published, and his publications include a textbook on International Pharmaceutical Registration, Active Pharmaceutical Ingredients and as Swiss correspondent to the Regulatory Affairs Journals Pharma and Medtech. Since 2012 he has been a member of the Editorial Board, Scrip Regulatory Affairs.<\/p>\n<p>\nFor more information about this conference visit <a target=\"_blank\" href=\"https:\/\/www.researchandmarkets.com\/reports\/5725561\/pharmaceutical-regulatory-affairs-in-asia?utm_source=BW&amp;utm_medium=PressRelease&amp;utm_code=v2pwpt&amp;utm_campaign=1816161+-+Final+Weeks+to+Register%3A+2+Day+Pharmaceutical+Regulatory+Affairs+in+Asia+Training+Course+-+All+Important+Aspects+of+Gaining+and+Maintaining+a+Successful+Marketing+Authorisation+(June+14-16%2C+2023)&amp;utm_exec=chdo54prd\" rel=\"nofollow noopener\" shape=\"rect\">https:\/\/www.researchandmarkets.com\/r\/ylz978<\/a><\/p>\n<p>\n<strong>About ResearchAndMarkets.com<\/strong><\/p>\n<p>\nResearchAndMarkets.com is the world&#8217;s leading source for international market research reports and market data. We provide you with the latest data on international and regional markets, key industries, the top companies, new products and the latest trends.<\/p>\n<p> <b>Contacts<\/b> <\/p>\n<p>\nResearchAndMarkets.com<br \/>\n<br \/>Laura Wood, Senior Press Manager<br \/>\n<br \/><a target=\"_blank\" href=\"&#109;&#x61;&#105;&#x6c;&#116;&#x6f;&#58;&#x70;&#114;&#x65;&#115;&#x73;&#64;&#x72;e&#x73;e&#x61;r&#x63;h&#x61;n&#100;&#x6d;&#97;&#x72;&#107;&#x65;&#116;&#x73;&#46;&#x63;&#111;&#x6d;\" rel=\"nofollow noopener\" shape=\"rect\">&#112;&#x72;e&#115;&#x73;&#64;&#114;&#x65;s&#101;&#x61;r&#99;&#x68;a&#110;&#x64;m&#97;&#x72;k&#101;&#x74;s&#46;&#x63;o&#109;<\/a><\/p>\n<p>For E.S.T Office Hours Call 1-917-300-0470<br \/>\n<br \/>For U.S.\/ CAN Toll Free Call 1-800-526-8630<br \/>\n<br \/>For GMT Office Hours Call +353-1-416-8900<\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>DUBLIN&#8211;(BUSINESS WIRE)&#8211;The &#8220;Pharmaceutical Regulatory Affairs in Asia Training Course&#8221; conference has been added to ResearchAndMarkets.com&#8217;s offering. This seminar will provide a practical overview of the key areas of pharmaceutical regulatory affairs in Asia, including India, and will cover all important aspects of gaining and maintaining a successful marketing authorisation within the region. The pharmaceutical market &#8230; <span class=\"more\"><a class=\"more-link\" href=\"https:\/\/pharma-trend.com\/en\/final-weeks-to-register-2-day-pharmaceutical-regulatory-affairs-in-asia-training-course-all-important-aspects-of-gaining-and-maintaining-a-successful-marketing-authorisation-june-14-16-2023-re\/\">[Read more&#8230;]<\/a><\/span><\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[13],"tags":[],"class_list":{"0":"entry","1":"post","2":"publish","3":"author-business","4":"post-55626","6":"format-standard","7":"category-industry"},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Final Weeks to Register: 2 Day Pharmaceutical Regulatory Affairs in Asia Training Course - All Important Aspects of Gaining and Maintaining a Successful Marketing Authorisation (June 14-16, 2023) - ResearchAndMarkets.com - Pharma Trend<\/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:\/\/pharma-trend.com\/en\/final-weeks-to-register-2-day-pharmaceutical-regulatory-affairs-in-asia-training-course-all-important-aspects-of-gaining-and-maintaining-a-successful-marketing-authorisation-june-14-16-2023-re\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Final Weeks to Register: 2 Day Pharmaceutical Regulatory Affairs in Asia Training Course - All Important Aspects of Gaining and Maintaining a Successful Marketing Authorisation (June 14-16, 2023) - ResearchAndMarkets.com - Pharma Trend\" \/>\n<meta property=\"og:description\" content=\"DUBLIN&#8211;(BUSINESS WIRE)&#8211;The &#8220;Pharmaceutical Regulatory Affairs in Asia Training Course&#8221; conference has been added to ResearchAndMarkets.com&#8217;s offering. 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This seminar will provide a practical overview of the key areas of pharmaceutical regulatory affairs in Asia, including India, and will cover all important aspects of gaining and maintaining a successful marketing authorisation within the region. The pharmaceutical market ... 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