Services
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Apollo™
8/18/2023
Apollo™ is an innovative platform that empowers you with real-time access to study data, milestones, documents, and program planning tools.
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SUREtechnology Platform™
8/4/2023
Explore how an advanced Cell Line Development (CLD) platform for new biologics can enable CHO-based cell line development; ensure premium, stable, and high-yield results; overcome common expression bottlenecks; and provide robust verification, genomic characterization, and monoclonality assessment services.
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Drug Substance Services
7/27/2023
Examine our drug product manufacturing capabilities and how our skilled scientists work with customers to build a chemical in a cost-effective and timely manner throughout the clinical development process.
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Integrated Drug Discovery
7/1/2023
Finding a partner with integrated services is crucial for accelerating timelines and accessing solutions with comprehensive expertise, all while removing risk from the drug product lifecycle.
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AGCellerate For mAbs
6/29/2023
AGC Biologics has released a new program designed to deliver effective IND-ready GMP material for biopharmaceutical developers. AGCellerate offers guaranteed amounts at fixed timelines and costs –accelerating projects through development and into clinical phases.
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Safety Assessment Services
6/20/2023
A full range of in vivo and in vitro testing services that can be customized for your project’s needs to expedite preclinical development while maintaining a high quality standard.
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One Step
6/20/2023
Make strides with a tailored, comprehensive suite of discovery and development services to rapidly progress your project and reduce time to market.
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PUREplatform PUREcoli, A Pure Microbial Strain For Protein Production
3/17/2023
PUREplatform offers a platform, a premium strain, and cutting-edge screening, which together yield optimal protein expression that is uniquely tailored to each project.
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Process Development: Mammalian, Bacteria And Yeast Based Success
2/17/2022
At AGC Biologics, we have developed over 200 mammalian, bacteria and yeast-based processes, giving us the insight necessary to identify and optimize process parameters that are critical for achieving a high-quality, cost-effective manufacturing process.
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cGMP Aseptic Manufacturing And Sterile Fill-Finish
1/28/2022
Experienced CDMOs will implement a cGMP aseptic manufacturing and sterile fill-finish policy to improve drug bioavailability. Aseptic fill-finish is a process in which the drug product, container, and container closure are sterilized separately and then integrated. Combining the drug, container, and closure in a clean room using special equipment that is self-contained in a sterile environment meets FDA guidelines related to cGMP.