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China Resources Boya Bio pharmaceutical Group Co Ltd

China Resources Boya Bio-pharmaceutical Group Co., Ltd. researches, develops, produces, and sells blood products in China. Its offerings include human serum albumin, various immunoglobulins (human, intravenous, freeze-dried intravenous, hepatitis B, tetanus, and rabies), human fibrinogen, prothrombin complex, and coagulation factor VIII. The company also provides compound bone peptide, oxytocin, heparin sodium injection, posterior pituitary, and carboprost tromethamine injection, as well as anti-infective, diabetes, and cardiovascular drugs. Formerly known as Boya Bio-pharmaceutical Group Co., Ltd., it changed its name to China Resources Boya Bio-pharmaceutical Group Co., Ltd. Founded in 1993, the company is based in Fuzhou, China.

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Boya Bio's 2026 interim net profit was 51.19 million yuan, down 77.28% year-on-year

Boya Bio released its 2026 interim report, with net profit attributable to the parent company of 51.19 million yuan, a year-on-year decrease of 77.28%. The company's total operating revenue was 644 million yuan, down 36.14% year-on-year; net cash flow from operating activities was negative 136 million yuan, down 2,062.30% year-on-year. The company's latest asset-liability ratio was 10.15%, gross margin was 44.21%, ROE was 0.69%, and diluted earnings per share was 0.10 yuan.
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Boya Bio's Dalad Banner Plasma Collection Station Approved for Operation

China Resources Boya Bio-pharmaceutical Group's controlled subsidiary, Dalad Banner Boya Plasma Collection Co., Ltd., has obtained a Plasma Collection License from the Health Commission of Inner Mongolia Autonomous Region, granting approval to operate. The station is located in Dalad Banner, Ordos City, Inner Mongolia, with a collection area limited to the Dalad Banner region. Its business scope covers the collection and supply of source plasma, and the license is valid from July 17, 2026 to July 16, 2028. The company stated that obtaining the license and approval to operate will help enhance its source plasma supply capacity and have a positive impact on its long-term development.
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Biotech & Genomic Medicine2

Boya Bio's Human von Willebrand Factor Re-Approved for Clinical Trials After Process Upgrade

China Resources Boya Bio-pharmaceutical Group's human von Willebrand factor has received a renewed drug clinical trial approval notice from the National Medical Products Administration on July 20, 2026, following an upgrade to its core manufacturing process. The product is intended for treating spontaneous and trauma-induced bleeding in adult and adolescent patients with von Willebrand disease. It first obtained clinical trial approval in August 2021, and the process upgrade was subsequently carried out to enhance product quality stability and clinical safety, with a new application submitted in April 2026. As of the announcement date, cumulative R&D investment in the project is approximately 41 million yuan. Currently, no similar product independently developed by a domestic company has been approved for marketing in China. The company stated that this approval will strengthen its pipeline for rare bleeding disorders, but the project remains in the clinical stage and will not have a significant impact on its 2026 operating results.
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