{"id":61239,"date":"2025-05-12T16:02:18","date_gmt":"2025-05-12T14:02:18","guid":{"rendered":"https:\/\/pharma-trend.com\/en\/pharmaceutical-regulatory-affairs-in-china-2-day-online-training-course-june-25-26-2025-unlock-pharmaceutical-success-in-china-researchandmarkets-com\/"},"modified":"2025-05-12T16:02:18","modified_gmt":"2025-05-12T14:02:18","slug":"pharmaceutical-regulatory-affairs-in-china-2-day-online-training-course-june-25-26-2025-unlock-pharmaceutical-success-in-china-researchandmarkets-com","status":"publish","type":"post","link":"https:\/\/pharma-trend.com\/en\/pharmaceutical-regulatory-affairs-in-china-2-day-online-training-course-june-25-26-2025-unlock-pharmaceutical-success-in-china-researchandmarkets-com\/","title":{"rendered":"Pharmaceutical Regulatory Affairs in China &#8211; 2 Day Online Training Course (June 25-26, 2025) | Unlock Pharmaceutical Success in China &#8211; ResearchAndMarkets.com"},"content":{"rendered":"<div>\n<p>DUBLIN&#8211;(BUSINESS WIRE)&#8211;The <a target=\"_blank\" href=\"https:\/\/www.researchandmarkets.com\/reports\/6028869\/pharmaceutical-regulatory-affairs-in-china?utm_source=BW&amp;utm_medium=PressRelease&amp;utm_code=76cfzj&amp;utm_campaign=2061304+-+Pharmaceutical+Regulatory+Affairs+in+China+-+2+Day+Online+Training+Course+(June+25-26%2C+2025)+%7C+Unlock+Pharmaceutical+Success+in+China&amp;utm_exec=carimspi\" rel=\"nofollow\" shape=\"rect\">&#8220;Pharmaceutical Regulatory Affairs in China Training Course (ONLINE EVENT: June 25-26, 2025)&#8221;<\/a> has been added to <strong>ResearchAndMarkets.com&#8217;s<\/strong> offering.\n<\/p>\n<p><a href=\"https:\/\/mms.businesswire.com\/media\/20250512175220\/en\/2466468\/4\/logo.jpg\"><img decoding=\"async\" src=\"https:\/\/mms.businesswire.com\/media\/20250512175220\/en\/2466468\/22\/logo.jpg\"><\/a><br \/><a href=\"https:\/\/mms.businesswire.com\/media\/20250512175220\/en\/2466468\/4\/logo.jpg\"><img decoding=\"async\" src=\"https:\/\/mms.businesswire.com\/media\/20250512175220\/en\/2466468\/21\/logo.jpg\"><\/a><\/p>\n<p>\nExplore the comprehensive landscape of pharmaceutical marketing authorization in China, including Hong Kong, Macau, and Taiwan, through this specialized two-day seminar.\n<\/p>\n<p>\nThis seminar will provide an invaluable overview of how to gain and maintain a successful pharmaceutical marketing authorisation in the People&#8217;s Republic of China (PRC), including Hong Kong, Macau and Taiwan.\n<\/p>\n<p>\n<strong>The two-day course will cover:<\/strong>\n<\/p>\n<ul>\n<li>\nAll important aspects of gaining and maintaining a successful marketing authorisation in the region\n<\/li>\n<li>\nRecent regulatory reforms\n<\/li>\n<li>\nDrug regulatory systems\n<\/li>\n<li>\nAn overview of import and local manufacture registration\n<\/li>\n<li>\nClinical product development including CMC regulatory requirements\n<\/li>\n<li>\nAn interpretation of practical aspects\n<\/li>\n<li>\nThe opportunity to exchange experiences with other delegates\n<\/li>\n<\/ul>\n<p>\n<strong>Benefits of attending:<\/strong>\n<\/p>\n<ul>\n<li>\n<strong>Gain<\/strong> an overview of the regulatory procedures in the region\n<\/li>\n<li>\n<strong>Understand<\/strong> and assess the impact of recent regulatory reforms\n<\/li>\n<li>\n<strong>Discuss<\/strong> clinical product development and Chinese-specific approaches\n<\/li>\n<li>\n<strong>Understand<\/strong> requirements for import and local manufacturing registration\n<\/li>\n<li>\n<strong>Discuss<\/strong> product registration strategies\n<\/li>\n<\/ul>\n<p>\n<strong>Who Should Attend:<\/strong>\n<\/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 in this region. You will find this seminar useful both as an introductory or refresher course.\n<\/p>\n<p>\nPrevious delegates have included scientists and technical staff in regulatory affairs and registration departments, medical directors, and personnel from analytical research and development, clinical development, quality assurance, new business development and regulatory authorities.\n<\/p>\n<p>\n<strong>Certifications:<\/strong>\n<\/p>\n<ul>\n<li>\nCPD: 12 hours for your records\n<\/li>\n<li>\nCertificate of completion\n<\/li>\n<\/ul>\n<p>\n<strong>Course Agenda:<\/strong>\n<\/p>\n<p>\n<strong>Day 1<\/strong>\n<\/p>\n<p>\n<strong>General introduction to the PRC and the pharmaceutical market<\/strong>\n<\/p>\n<ul>\n<li>\nCommercial and cultural background\n<\/li>\n<\/ul>\n<p>\n<strong>P.R. China &#8211; Drug Regulatory Systems<\/strong>\n<\/p>\n<ul>\n<li>\nRegulatory authorities\n<\/li>\n<li>\nRecent regulatory changes\n<\/li>\n<li>\nRegulations and guidelines\n<\/li>\n<li>\nDrug classification systems\n<\/li>\n<li>\nImport and local manufacturing registration\n<\/li>\n<li>\nData requirements\n<\/li>\n<li>\nRegistration requirements\n<\/li>\n<li>\nLabelling requirements\n<\/li>\n<\/ul>\n<p>\n<strong>P.R. China &#8211; Clinical Product Development<\/strong>\n<\/p>\n<ul>\n<li>\nRegulatory aspects of clinical development\n<\/li>\n<li>\nRecent regulatory changes\n<\/li>\n<li>\nDocumentation needs including CMC\n<\/li>\n<li>\nRegulatory requirements including GCP aspects\n<\/li>\n<li>\nChinese-specific approaches\n<\/li>\n<li>\nMultinational clinical trials\n<\/li>\n<\/ul>\n<p>\n<strong>Hong Kong SAR<\/strong>\n<\/p>\n<ul>\n<li>\nBackground overview\n<\/li>\n<li>\nRegulatory authorities\n<\/li>\n<li>\nRegulatory requirements and procedures\n<\/li>\n<li>\nSpecific market aspects\n<\/li>\n<\/ul>\n<p>\n<strong>Macau SAR<\/strong>\n<\/p>\n<ul>\n<li>\nBrief overview of regulatory aspects\n<\/li>\n<\/ul>\n<p>\n<strong>Day 2<\/strong>\n<\/p>\n<p>\n<strong>P.R. China &#8211; Regulatory Strategies<\/strong>\n<\/p>\n<p>\n<strong>P.R. China &#8211; Health Authority Interactions<\/strong>\n<\/p>\n<p>\n<strong>P.R. China &#8211; Maintenance<\/strong>\n<\/p>\n<p>\n<strong>Taiwan (Republic of China)<\/strong>\n<\/p>\n<ul>\n<li>\nCultural background\n<\/li>\n<li>\nRegulatory authorities\n<\/li>\n<li>\nRegulations and guidelines\n<\/li>\n<li>\nDrug classification systems\n<\/li>\n<li>\nData requirements\n<\/li>\n<li>\nCountry-specific matters\n<\/li>\n<\/ul>\n<p>\n<strong>P.R China &#8211; Recent Developments<\/strong>\n<\/p>\n<p>\nFor more information about this training course visit <a target=\"_blank\" href=\"https:\/\/www.researchandmarkets.com\/reports\/6028869\/pharmaceutical-regulatory-affairs-in-china?utm_source=BW&amp;utm_medium=PressRelease&amp;utm_code=76cfzj&amp;utm_campaign=2061304+-+Pharmaceutical+Regulatory+Affairs+in+China+-+2+Day+Online+Training+Course+(June+25-26%2C+2025)+%7C+Unlock+Pharmaceutical+Success+in+China&amp;utm_exec=carimspi\" rel=\"nofollow\" shape=\"rect\">https:\/\/www.researchandmarkets.com\/r\/xr9sn9<\/a>\n<\/p>\n<p>\n<strong>About ResearchAndMarkets.com<\/strong>\n<\/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.\n<\/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=\"&#x6d;a&#x69;&#108;&#x74;&#111;&#x3a;&#x70;r&#x65;&#115;&#x73;&#64;&#x72;&#101;s&#x65;&#97;&#x72;&#99;&#x68;&#97;n&#x64;&#109;&#x61;&#114;&#x6b;&#101;t&#x73;&#46;&#x63;&#111;&#x6d;\" rel=\"nofollow\" shape=\"rect\">&#x70;&#x72;&#x65;&#x73;&#115;&#64;&#114;&#101;sea&#x72;&#x63;&#x68;&#x61;&#x6e;&#100;&#109;&#97;rke&#x74;&#x73;&#x2e;&#x63;&#x6f;&#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\n<\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>DUBLIN&#8211;(BUSINESS WIRE)&#8211;The &#8220;Pharmaceutical Regulatory Affairs in China Training Course (ONLINE EVENT: June 25-26, 2025)&#8221; has been added to ResearchAndMarkets.com&#8217;s offering. Explore the comprehensive landscape of pharmaceutical marketing authorization in China, including Hong Kong, Macau, and Taiwan, through this specialized two-day seminar. This seminar will provide an invaluable overview of how to gain and maintain a &#8230; <span class=\"more\"><a class=\"more-link\" href=\"https:\/\/pharma-trend.com\/en\/pharmaceutical-regulatory-affairs-in-china-2-day-online-training-course-june-25-26-2025-unlock-pharmaceutical-success-in-china-researchandmarkets-com\/\">[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-61239","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>Pharmaceutical Regulatory Affairs in China - 2 Day Online Training Course (June 25-26, 2025) | Unlock Pharmaceutical Success in China - 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\/pharmaceutical-regulatory-affairs-in-china-2-day-online-training-course-june-25-26-2025-unlock-pharmaceutical-success-in-china-researchandmarkets-com\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Pharmaceutical Regulatory Affairs in China - 2 Day Online Training Course (June 25-26, 2025) | Unlock Pharmaceutical Success in China - ResearchAndMarkets.com - Pharma Trend\" \/>\n<meta property=\"og:description\" content=\"DUBLIN&#8211;(BUSINESS WIRE)&#8211;The &#8220;Pharmaceutical Regulatory Affairs in China Training Course (ONLINE EVENT: June 25-26, 2025)&#8221; has been added to ResearchAndMarkets.com&#8217;s offering. 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