{"id":7822,"date":"2024-03-14T22:49:48","date_gmt":"2024-03-14T14:49:48","guid":{"rendered":"https:\/\/flcube.com\/?p=7822"},"modified":"2024-10-18T22:51:45","modified_gmt":"2024-10-18T14:51:45","slug":"shanghai-unveils-17-measures-to-enhance-medical-administration-business-environment","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=7822","title":{"rendered":"Shanghai Unveils 17 Measures to Enhance Medical Administration Business Environment"},"content":{"rendered":"\n

Shanghai\u2019s Medical Product Administration has unveiled a comprehensive set of 17 measures aimed at fostering a world-class business environment in the medical administration sector. The initiatives focus on enhancing service levels, advancing benchmarking reforms, and optimizing regulatory supervision.<\/p>\n\n\n\n

Key measures include:<\/p>\n\n\n\n

    \n
  1. Streamlined Services: Accelerating the registration and implementation of drugs and medical devices through a refined “one list, two optimizations” service mechanism tailored to meet enterprise needs for regulatory policies and technical evaluations.<\/li>\n\n\n\n
  2. Optimized Registration Guidance: Enhancing guidance for innovative medical devices, including pre-application services for Class II devices undergoing special review processes, and implementing pre-examination for first-time registration materials.<\/li>\n\n\n\n
  3. Proactive Cosmetics Guidance: Strengthening support services for cosmetic product regulation.<\/li>\n\n\n\n
  4. Key Enterprise Support: Establishing a dynamic service package for key enterprises, implementing tailored policies for critical products.<\/li>\n\n\n\n
  5. Registration Guidance Workstations: Launching Version 2.0 of the Guiding Opinions for Biomedical Product Registration Guidance Service Workstations to support innovative product development and provide daily consulting services.<\/li>\n\n\n\n
  6. Clinical Trial Support: Improving capabilities for conducting international multicenter clinical trials and establishing a robust information-based supervision mechanism.<\/li>\n\n\n\n
  7. Port Supply Policies: Exploring policies for the supply of drugs and medical equipment for international cruise ships at ports.<\/li>\n\n\n\n
  8. Biological Product Production: Piloting segmented production processes for biopharmaceuticals with urgent clinical needs.<\/li>\n\n\n\n
  9. Continuous Manufacturing Technology: Promoting the industrial application of advanced technologies in continuous pharmaceutical manufacturing.<\/li>\n\n\n\n
  10. Drug Supplement Applications: Streamlining the process for optimizing supplementary drug applications.<\/li>\n\n\n\n
  11. Medical Device Registration: Reducing the average technical evaluation time for Class II medical devices to 55 working days by the end of 2024.<\/li>\n\n\n\n
  12. Intelligent Government Services: Enhancing the intelligence level of government services.<\/li>\n\n\n\n
  13. Retail Pharmacy Supervision: Implementing “Internet plus” supervision to improve collaborative oversight across departments.<\/li>\n\n\n\n
  14. Yangtze River Delta Collaboration: Promoting cross-regional cooperation in the supervision of drug production and cosmetic registrants.<\/li>\n\n\n\n
  15. Credit Rating Supervision: Implementing dynamic classification and grading supervision based on credit and risk assessments.<\/li>\n\n\n\n
  16. Compliance Guidelines: Providing risk warnings for common regulatory violations and promoting self-inspection among enterprises.<\/li>\n\n\n\n
  17. In-Process Supervision: Enforcing a fault-tolerant mechanism for first violations and minimizing administrative penalties for minor infractions in the pharmaceutical sector.- Flcube.com<\/a><\/li>\n<\/ol>\n\n\n\n

    <\/p>\n","protected":false},"excerpt":{"rendered":"

    Shanghai\u2019s Medical Product Administration has unveiled a comprehensive set of 17 measures aimed at fostering…<\/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":[14],"class_list":["post-7822","post","type-post","status-publish","format-standard","hentry","category-policy-regulatory","tag-nmpa"],"yoast_head":"\nShanghai Unveils 17 Measures to Enhance Medical Administration Business Environment - Insight, China's Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"Shanghai\u2019s Medical Product Administration has unveiled a comprehensive set of 17 measures aimed at fostering a world-class business environment in the medical administration sector. 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