揚帆出海,向海圖強。當中國醫藥產品走向更廣闊的全球市場,好品質的標尺如何劃定?揚子江藥業集團(以下簡稱揚子江)正用中國質量的硬核實力給出答案——成為全球公眾健康的可靠選項。
2025年,這家發源于長江之濱的民族藥企,實現歷史性突破——成為首家通過世界三大質量獎之一“EFQM全球獎”RbE現場評審“七星”認證的中國藥企。質量實力的背后,是一套以“為父母制藥 為親人制藥”的質量文化為內核,貫通頂層設計與生產一線的全鏈條管理體系。揚子江將EFQM模型、“大質量”理念深度嵌入從原料種植、生產制造到流通服務的全過程,牢牢把握對“好”質量的主動權。旗下多個車間和品種接連通過歐盟EMA、美國FDA、日本PMDA等國際權威認證。今年4月,喜訊再次傳來,揚子江一次性通過烏干達GMP核查,這也是其在非洲市場的首個官方現場認證,國際化戰略在非洲大陸落下關鍵一子。
憑借數十年的質量堅守、體系建設、品牌打造與創新突破,揚子江的質量建設成果獲得全球市場的信任。2025年全年,揚子江國際化營收同比增長超4倍,合作伙伴數量增長逾2倍,百余品種出口至40多個國家和地區,覆蓋歐洲、北美、亞太等主流市場,持續書寫中國醫藥質量的時代答卷。
獲得國際認可,只是起點。參與全球質量標準建設,是更深層的突破。揚子江參與起草的5項中藥材質量標準被正式錄入《歐洲藥典》;位于中國福建福鼎的梔子基地、內蒙古土默特的有機黃芪基地,均通過世界衛生組織認可的GACP認證。從藥材標準到種植源頭,中國醫藥質量正與全球規則展開全面接軌。
“讓‘好’能力走出去,是更高層次的國際化。”揚子江相關負責人表示。在烏干達,揚子江團隊正為當地藥企提供工業生產技術支持,助力提升當地醫藥制造產業水平;在老撾,企業規劃建設胖大海種植基地,既從源頭保障原料品質,也帶動當地產業升級。目前,揚子江的多項工業技術服務正在全球同步推進,實現從產品輸出向質量管理體系與技術輸出的延伸,筑強全球生態“共贏鏈”。
2026年是揚子江“國際化元年”,是向全球市場縱深布局、實現突破性發展的新起點。企業以質量為錨、向海而行的成長軌跡,是中國民族工業向上攀登、與世界共進的生動縮影——正如其多年質量實踐所印證的:真正的好質量,既要自身過硬,更要成就他人、惠及世界。

媒體報道
China’s Yangtze River Pharmaceutical Group Expands Global Footprint as Quality Drives Growth
In 2025, Yangtze River Pharmaceutical Group (YRPG) made significant progress in both global growth and quality initiatives. The company’s international revenue increased more than fourfold year over year, while the number of its global partners more than doubled. Over 100 products were exported to more than 40 countries and regions across Europe, North America, and the Asia-Pacific, further broadening the company’s presence.
This growth is supported by sustained international recognition of YRPG’s quality system. In 2025, the company became the first Chinese pharmaceutical firm to receive Seven-Star certification under the EFQM Recognised by Excellence (RbE) framework, a globally used management assessment model from the European Foundation for Quality Management. Its quality framework is built on a philosophy of “Making medicines by considering customers as our parents and loved ones,” embedded across the full value chain and combining the EFQM model with an integrated, end-to-end quality management approach from raw materials to distribution.
YRPG’s quality system continues to be validated by global regulators, with facilities and products certified by the EMA, FDA, and PMDA. In April, the company also passed a GMP inspection in Uganda on its first attempt, marking its first on-site certification in Africa and supporting further expansion in the region.
Beyond international recognition, YRPG is actively contributing to the development of global quality standards. Five traditional Chinese medicinal material quality standards co-developed by the company have been included in the European Pharmacopoeia. Its Gardenia cultivation base in Fuding, Fujian Province, and its organic Astragalus base in Tumed Right Banner, Inner Mongolia, have both obtained WHO-recognized GACP certification. From raw materials to cultivation, YRPG continues to align its quality system with international benchmarks.
In Uganda, YRPG provides production and technical support to local manufacturers. In Laos, it plans to establish a Pangdahai cultivation base to secure raw material quality and support local industry development. The company is also extending its industrial technical services globally, moving beyond product supply to include quality management systems and technology transfer, contributing to a more resilient global partnership ecosystem.
2026 marks a new phase in YRPG’s global roadmap, signaling a deeper push into international markets and a shift toward sustained, multi-market operations. As pharmaceutical markets evolve, quality, compliance, and supply reliability remain central. Anchored in quality, the company is expanding its products, standards, technologies, and services to support global public health.
關于揚子江藥業集團
長江為魂,蒼生為念,奔騰不息的揚子江,孕育滋養了以“求索進取,護佑眾生”為使命的揚子江藥業集團。
創建于1971年的揚子江藥業集團,是科技部命名的全國首批創新型企業,總部位于江蘇省泰州市,現有員工19000余人,旗下子公司分布泰州、北京、上海、南京、廣州、成都、蘇州、常州等地。主要產品中西藥并舉,拓展生物藥、醫療器械、大健康業務,部分產品出口至全球40多個國家和地區。
堅守質量,揚子江永恒不變的生命線。集團踐行“高質 惠民 創新 至善”的核心價值觀,視患者如親人,追求卓越品質,致力向社會提供優質高效的藥品和健康服務。至今蟬聯全國醫藥行業質量管理QC成果評比一等獎總數“二十一連冠”,累計斬獲36項國際質量管理小組會議(ICQCC)QC金獎;2次榮獲“中國質量獎提名獎”,3次奪得中國品牌價值評價醫藥健康板塊品牌價值、品牌強度“雙第一”。入選全國首批卓越級智能工廠。2021年,集團榮獲全球三大質量獎之一的EFQM全球獎;2025年4月,獲 EFQM RbE現場評審七星認證;成為迄今國內醫藥行業唯一獲此大獎的制藥企業。
創新驅動,揚子江奔騰不息的原動力。集團把創新作為高質量發展的戰略基點,實施中藥、化學藥、生物藥“三藥并舉”研發戰略,加快培育醫藥健康新質生產力。建成4個國家級創新平臺;擁有40個獨家中藥品種;2021年,首個自主研發的1類化學創新藥注射用磷酸左奧硝唑酯二鈉獲批上市;2024年,1.1類中藥創新藥益氣通竅丸上市;2025年,1類化學創新藥鹽酸妥諾達非片上市獲批。至今累計180多個仿制藥品種通過或視同通過質量和療效一致性評價。相繼榮獲3項國家科技進步二等獎;研究起草的5項中藥材質量標準被錄入《歐洲藥典》。
責任同行,揚子江護佑眾生勇擔當。集團連續多年鼎力支持醫學科技進步;第一時間馳援賑災;發揮產業優勢助力鄉村全面振興;熱心體育公益事業,廣泛支持健康促進;捐資設立三大慈善基金會……揚子江人在公益道路上向善而行。
展望未來,奮進中的揚子江藥業集團,與時代同頻,與相關方攜手同行,踐行“健康營銷 營銷健康”雙健康戰略,沿著高質量、可持續發展之路,推動“藥、醫、養、食、游”融合發展,深耕大健康和國際化,貢獻全人類健康福祉,努力向“做中國領先、世界一流的醫藥健康產業集團”的愿景邁進。
