New Start in 2025 | Shanghai Hycells Biotechnology and Shandong Qidu Biotechnology Sign Strategic Cooperation Agreement


 

 

New Start in 2025

 

 

 

On January 18, 2025, Shanghai Hycells Biotechnology and Shandong Qidu Biotechnology signed a strategic cooperation agreement to jointly pursue product development initiatives. Since its establishment, Hycells has been committed to providing customers with integrated solutions for the R&D, manufacturing, sales, and service of primary immune cell products. Leveraging cutting-edge biotechnology and a robust R&D team, and supported by its cell bank and culture media R&D platform, the company offers a comprehensive suite of customized services for immune cells, stem cells, and related cell culture media.

 

Shandong Qidu Biopharmaceutical Co., Ltd. is a biopharmaceutical company dedicated to the research and development of cutting-edge biopharmaceutical technologies and products, renowned throughout the industry for its superior product quality and strong market competitiveness. The company has established the Zibo City Cell Medicine Engineering Technology Research Center, which includes a high-standard, over-1,000-square-meter cell medicine cleanroom and a production line capable of manufacturing 5 million vials of high-end liquid culture media annually. It has thus developed three core technology platforms: a liquid culture media R&D platform, a cell medicine research platform, and an in vitro diagnostic reagent technology platform for self-testing systems.

 

Immune cell and stem cell culture media are indispensable critical raw materials in biopharmaceutical manufacturing, and their quality and stability directly impact the quality and safety of the final product. To meet the growing market demand for high-quality immune cell culture media while enhancing the production efficiency and market competitiveness of both companies, Hycells Biotechnology and Shandong Qidu Biotechnology have decided to collaborate. Under the agreement, the two parties will engage in joint innovation in the field of immune cell and stem cell culture media, jointly pursue cutting-edge technologies, tackle key technological challenges through R&D, and deepen industry–university–research collaboration, thereby collectively advancing forward-looking technological planning and driving product transformation and upgrading. This collaboration aims to integrate the high-quality resources of both parties and leverage their respective strengths, thereby enhancing the production efficiency and market competitiveness of both companies and actively fostering the high-quality development of the biopharmaceutical industry.

 

 1 (2).jpg
33.jpg

Photo from the Signing and Exchange Ceremony

 

Looking ahead, Hycells Biotechnology and Shandong Qidu Biotechnology will continue to deepen their collaboration, expand into new areas of cooperation, and jointly explore new opportunities in the biopharmaceutical industry.

 

3.jpg
5.jpg

Mr. Ren, General Manager of Shandong Qidu Bio (far left), and Mr. Zhou, General Manager of Hycells Bio (far right)

Official Signing Ceremony

 

The cooperation signing ceremony has concluded, Mr. Ren, General Manager of Shandong Qidu Biopharmaceutical Co., Ltd., presented Hycells Bio with a special gift: a 2025 “Abundance Through the Four Seasons” display plate from Huaguang National Porcelain, symbolizing harmony among heaven, earth, and humanity and the enduring blessings of fortune and prosperity. Blessings to us, and blessings to you as well. The Snake Offers Rui Ruyi, spring sunshine shines; may your home be filled with harmony, prosperity, and good fortune in all four seasons!

 

4.jpg

The photo shows the scene of the “Blessings Abound in All Four Seasons” plating ceremony.

 

 

 

Related News


HiXpan® Cell Culture Additive: Answers to Key Questions (Part 2)

Hycell’s maximum production capacity per batch is 200–400 units of the 500 mL format, ensuring stable supply and meeting customers’ ongoing production needs.


HiXpan® Cell Culture Additive: Key Questions and Answers (Part 1)

The blood‑derived raw materials used in HiXpan® cell culture additives comply with all regulatory requirements throughout collection, ethical review, informed consent, and commercial authorization, and are supported by a fully traceable supply chain.


(3) Batch Stability and Performance Verification | Upholding Quality, Striving for Progress While Maintaining Stability

This paper focuses on how Hycells transforms biological variability into engineering‑level determinism through a scientifically informed blending strategy and stringent control at the collection end.


(II) Security Assurance Section | Safety First, Defense Prioritized

Compliance‑driven traceability establishes a clear “identity” for the product, but the real test lies in safety. While a multi‑donor pooling strategy ensures batch‑to‑batch consistency, it also inevitably elevates the risk of pathogen introduction. In the face of these associated risks and challenges, Heyousheng has never compromised on its manufacturing standards—relying on more precise design to deliver on its promise of enhanced safety.


(1) Compliance and Traceability Section | Establishing a Foundation of Compliance, Ensuring Source Tracing

This article will examine how Hycells proactively integrates the quality management system into the hospital setting, translating compliance requirements into concrete, actionable practices starting at the sample collection stage, thereby establishing a trust‑based chain that can withstand audit scrutiny.


Compliance as the Foundation, Safety as the Core | The Steadfast Commitment and Confidence Behind Heyou Sheng’s Serum Substitute

In selecting hPL raw materials, Heyousheng consistently upholds the principle that “safety is determined at the source.” The samples used in production are rigorously collected in accordance with applicable standards and undergo stringent donor screening, effectively mitigating the risk of disease transmission at the very outset. Moreover, from informed consent forms and ethical approvals to clinical‑grade collection under the GCP framework, Heyousheng has established a fully traceable documentation chain, ensuring that every sample is accounted for and verifiable. In contrast to the industry’s longstanding reliance on the conventional model of using expired blood supplies from blood banks, this approach represents a structural, generational upgrade.