{"id":26709,"date":"2022-08-18T09:34:00","date_gmt":"2022-08-18T01:34:00","guid":{"rendered":"https:\/\/flcube.com\/?p=26709"},"modified":"2025-02-14T09:37:28","modified_gmt":"2025-02-14T01:37:28","slug":"cde-releases-draft-guidelines-for-rwe-backed-drug-registration-applications","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=26709","title":{"rendered":"CDE Releases Draft Guidelines for RWE-Backed Drug Registration Applications"},"content":{"rendered":"\n<p>The Center for Drug Evaluation (CDE) has released a notification regarding the \u201cReal-World Evidence (RWE)-backed Drug Registration Application Communication Guidelines\u201d (draft proposal). The draft is open for public feedback for one month. The aim is to provide specific requirements and guiding suggestions for communication between the applicant and the review agency to support registration applications with real-world evidence.<\/p>\n\n\n\n<p><strong>Background<\/strong><br>With the release of real-world evidence and real-world data guidelines, applicants have become more active in conducting real-world research. Communication with the CDE about conducting such research has also increased. The drafting group of the guideline is based on the tripartite academic coordination committee established by the CDE and Southern Medical University. The committee was initiated in March 2022 and held two expert seminars in March and May. These seminars fully discussed the first draft, which was reviewed internally by the CDE to form the draft proposal.<\/p>\n\n\n\n<p><strong>Core Issues Discussed<\/strong><br>The core issues discussed at the communication meeting include:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Consideration of the necessity and feasibility of conducting real-world research<\/li>\n\n\n\n<li>Clarifying the key elements of the research plan involved in communication<\/li>\n\n\n\n<li>Focusing on the applicability of real-world data<\/li>\n\n\n\n<li>The transparency of conducting real-world research<\/li>\n<\/ul>\n\n\n\n<p><strong>Materials Requirements<\/strong><br>Materials requirements pivot around the research implementation process. They clarify the relevant documents and specific requirements that should be prepared for communication prior to research implementation, during the research, and before submitting the registration application.<a href=\"https:\/\/flcube.com\/\">-Fineline Info &amp; Tech<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>The Center for Drug Evaluation (CDE) has released a notification regarding the \u201cReal-World Evidence (RWE)-backed&#8230;<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"googlesitekit_rrm_CAownpewDA:productID":"","_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":false,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2}},"categories":[4],"tags":[102],"class_list":["post-26709","post","type-post","status-publish","format-standard","hentry","category-policy-regulatory","tag-cde"],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v23.6 (Yoast SEO v27.6) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>CDE Releases Draft Guidelines for RWE-Backed Drug Registration Applications - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"The Center for Drug Evaluation (CDE) has released a notification regarding the \u201cReal-World Evidence (RWE)-backed Drug Registration Application Communication Guidelines\u201d (draft proposal). The draft is open for public feedback for one month. The aim is to provide specific requirements and guiding suggestions for communication between the applicant and the review agency to support registration applications with real-world evidence.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/flcube.com\/?p=26709\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"CDE Releases Draft Guidelines for RWE-Backed Drug Registration Applications\" \/>\n<meta property=\"og:description\" content=\"Navigate the complexities of China\u2019s pharmaceutical industry with precision and clarity. FLCUBE delivers reliable data, news, and intelligence to broaden your horizons and sharpen your decision-making. 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