Allsino pharmaceutical Co., Ltd. Your Premier Partner in Small Molecule & Peptide CDMO Services Company Overview Founded in May 2004, Allsino Biopharmaceutical Co., Ltd.is a wholly-owned subsidiary of Sinopep-Allsino Biopharmaceutical Co., Ltd. (Stock Code: 688076), a publicly traded company on the Shanghai Stock Exchange’s STAR Market . Headquartered in Hangzhou, China, Allsino is a globally recognized Contract Development and Manufacturing Organization (CDMO), specializing in the research, development, and production of innovative small molecule drugs, advanced pharmaceutical intermediates, and peptide fragments. With a steadfast commitment to quality and innovation, Allsino serves as a critical bridge between early-stage drug discovery and commercial manufacturing, helping partners accelerate timelines and reduce risks. Strategic Locations: R&D and GMP Manufacturing Allsino operates an integrated Hangzhou R&D + Jiande Manufacturing” dual-site model to ensure seamless technology transfer and scalable production. R&D Center (Hangzhou, Zhejiang): Location: Yuhang District, Hangzhou. Status: Recognized as a Provincial Enterprise Research Institute by the Zhejiang Provincial Government . Capabilities: Houses over 100 scientists, including Ph.D. and Master’s level chemists. The center focuses on core technologies such as small molecule catalysis, continuous flow chemistry, and solid-phase peptide synthesis. – GMP Commercial Production Base (Jiande, Zhejiang): – Location:Jiande City, Hangzhou. – Scale: Spanning 60,000+ square meters(approx. 146 Mu) . – Certification: Operates under strict cGMP standards, compliant with US FDA, EDQM, and NMPA regulations . In 2023, the facility successfully passed the NMPA GMP evaluation for APIs . Core Business & Technical Expertise Allsino is an innovation-driven entity that has successfully initiated and developed over 300 projects across various therapeutic areas, including oncology, central nervous system (CNS) disorders, and metabolic diseases (including GLP-1 analogs for diabetes and obesity) . Key Services: Process Development & Scale-up: From laboratory synthesis to multi-ton commercial production. – Custom Synthesis: Advanced intermediates, Registered Starting Materials (RSMs), and GMP-grade Active Pharmaceutical Ingredients (APIs) . Peptide CDMO Services:Specializing in peptide fragments and oligonucleotides. Commercial Manufacturing: Supporting NDA filings and commercial launch. Quality & Global Recognition Allsino’s commitment to pharmaceutical excellence is validated by its long-standing partnerships with top-tier global pharmaceutical companies. Global Partnerships:The company has established long-term technical collaborations with Fortune 500 pharmaceutical companies such as ****** . Industry Award: In 2022, Allsino was honored with the “SK Pharmteco Preferred Partner Award” at CPhI Frankfurt. Notably, Allsino was the only Chinese company selected among nearly 100 global suppliers to receive this distinction . Intellectual Property: Holds over 20 patents (including inventions and utility models) . Certifications – US FDA (cGMP) – NMPA (China GMP) – ISO 9001, ISO 14001, ISO 45001 Workforce & Assets Employees:500+ , including a highly educated technical team of 240+ professionals (6 Ph.D.s, 16 Master’s degrees) . Annual R&D Investment: Consistently exceeds 10% of revenue, ensuring continuous technological innovation . Contact Information Website:[www.allsino.com](http://www.allsino.com) R&D Center Address: 4F, Building 1, No. 39 Keji Avenue, Yuhang District, Hangzhou, Zhejiang, China (Postal Code: 311121) Manufacturing Base Address:No. 18 Fenghe Road, Xiaya Town, Jiande City, Hangzhou, Zhejiang, China (Postal Code: 311606) Phone: +86-571-89961929 / +86-571-88180350 Email (Sales): sales@allsino.com Allsino pharmaceutical Co., Ltd.—Bridging Innovation from Lab to Market.
Agilent Advanced Therapeutics, fka BIOVECTRA
Agilent Advanced Therapeutics is Agilent’s contract development and manufacturing organization (CDMO), bringing together BIOVECTRA’s proven expertise in biologics fermentation, complex chemistry, highly potent APIs, and bioreagents, with Agilent’s Nucleic Acid Solutions Division capabilities in oligonucleotides and advanced nucleic acid manufacturing. Together, these complementary strengths create a unified CDMO partner supporting advanced therapeutics from development through commercial supply. Combining white-glove service, deep scientific expertise, and long-term investment, Agilent Advanced Therapeutics delivers customized end-to-end solutions designed around each client’s needs. Backed by rigorous, data-driven processes and Agilent’s global quality systems, our scientists work alongside yours to help move programs forward with confidence. Invested in science, invested in your success.
Abzena
Abzena is a bioconjugate- and biologics-focused CDMO that pushes development of novel treatments forward at every stage from discovery through commercial launch. With the ability to tailor its strategy and customer experience to each project, Abzena develops and implements innovative solutions that enable biotech and biopharma companies to realize the full potential of their investments in human health. The company has research, development, and cGMP facilities across locations in San Diego, CA, Bristol, PA, and Cambridge, UK. #bioconjugation #linkerpayloads #ADCs #Biologics # | Abzena is the leading end-to-end bioconjugate and complex biologics CDMO + CRO. From discovery through commercial launch, we support customers with fully integrated programs or individual services designed to de-risk and streamline the development of new treatments for patients in need. With the ability to tailor its strategy and customer experience to each project, Abzena develops and implements innovative solutions that enable biotech and biopharma companies to realize the full potential of their molecule and move medicines forward faster. The company has research, development, and cGMP facilities across locations in San Diego, CA, Bristol, PA, and Cambridge, UK. We provide comprehensive support for multiple modalities including: Antibodies (mAbs), FAbs, ADCs, Bispecifics, Radioconjugates, Fusion Proteins, Growth Factors, Vaccines, mRNA, Biosimilars, Peptide Oligonucleotides. Our capabilities range from: Early-Stage Research & Discovery, Design and Lead Selection, Robust Analytics, Bioassays and Immunogenicity, Antibody Engineering and Developability, Mammalian Cell Line Development, Linker Payload Design and Synthesis, Analytical Method & Formulation Development, Process Development and cGMP Manufacturing up to 2000L, Technology Transfer & Scale-Up, Regulatory Support Our extensive toolkit of services is designed to ensure our customers achieve their Target Product Profile (TPP). With early-stage research, process development and GMP manufacturing capabilities all under a single organization, we can leverage our vast capabilities and knowledge of the product, along with the requisite In Vitro and In Vivo criteria to ensure that the desired TPP can be accomplished from the project outset. | Abzena is the leading end-to-end bioconjugate (ADCs, AOCs, RDCs) and complex biologics CDMO + CRO. From discovery through commercial, we support customers with fully integrated programs or individual services that de-risk and streamline the development of new medicines. With over two decades of experience, 2000+ conjugates developed and over 200+ cell lines developed, we have the expertise and technical know-how to rapidly progress your biopharmaceutical to IND and beyond. And with footholds in the US and UK, we offer a simplified and secure supply chain. Fully integrated CDMO+CRO support across multiple modalities: Monoclonal Antibodies (mAbs), Antibody-Drug Conjugates (ADCs), Antibody-Oligonucleotide Conjugates (AOCs), Radionuclide Antibody-Conjugates (RACs) & Radionuclide Drug-Conjugates (RDCs),Bispecific Antibodies (bsAbs), Fusion Proteins, Cytokines, Recombinant & Conjugate Vaccines, Nanoparticles With Capabilities Ranging From: Early-Stage Research & Discovery, Design and Lead Selection, Robust Analytics, Bioassays and Immunogenicity, Bioconjugation & Chemistry, Antibody, Engineering and Developability, Mammalian Cell Line Development, Linker Payload Design and Synthesis, Analytical Method & Formulation Development, Process Development and cGMP Manufacturing up to 2000L, Technology Transfer & Scale-Up, Regulatory Support. Key Facts & Highlights: Over 24 years of experience developing 2000+ conjugations and 200+ cell lines. Champion Award Winner in Global Biologics at the 2025 CDMO Leadership Awards. Unique end-to-end value proposition ranging from antibody discovery to clinical-scale GMP biologic drug substance manufacture. Scientific expertise to deliver at high quality, low cost and compressed timelines. Global customer base, including most of the top 20 biopharmaceutical companies. Supply chain security with fully integrated US & UK facilities that can handle highly potent and cytotoxic molecules. 14 products utilizing Abzena’s technologies in clinical trials. Biologics discovery, design, optimization, characterization, lead selection, cell line development, process development & GMP manufacture for supply from preclinical through commercial scale. Bioconjugate (including ADCs, AOCs, RDCs) discovery, design, optimization, characterization, lead selection, cell line development, process development & GMP manufacture for supply from preclinical through commercial scale. Synthesis, analysis and GMP manufacture of APIs, payloads and highly potent compounds (HPAPI) and cytotoxic. Discovery to Phase II accelerated development for antibody-drug conjugates, including antibodies, linkers, and payloads. Tech transfer and commercial scale manufacturing up to 2000L for biologics and bioconjugates.