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Process and Analytical Method Development
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Process and Analytical Method Development
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Overview
Cell Culture
Process Development
Purification Process
Development
Drug Product
Formulation and
Lophilization Process
Analysis Services
Services
Drug substance analysis
Development, validation and transfer of analytical methods for drug substance
Characterization of in-house reference substance for biologicals
Development, validation and transfer of cell based activity assay methods
Drug substance release
Stability study
Quality study
Structural characterization of biologics and study on related substances
Higher order structure analysis for biologics
Charge variants analysis for biologics
Biosimilar similarity study
Comparability study of biologicals
Drug product analysis
Development, validation and transfer of analytical methods for drug product
Drug product release
Stability study
Compatibility study on package materials
Extractables/leachables study on single-use system
Other services
Release of raw materials and excipients
Microbial limit test
Sterility test
GMP facility validation and environmental monitoring support
Technical Capability
Biochemical analysis
Antigen-antibody binding activity assay
Residual HCP/DNA/Pro A test
Fc receptor binding activity assay
Gene copy number test
Mycoplasma test (Q-PCR)
Biological analysis
Cytotoxicity test
Fc function test (ADCC/CDC)
Immunofunction test
Report gene test
Gene expression determination
Virus content determination
Physicochemical characterization
Protein content
Purity (SEC/CE-SDS/HIC/RP)
Peptide map
Charge heterogeneity (IEC/iCIEF/CZE)
DAR (UV/HIC/RP)
N-glycan profile and sialic acid analysis
Residues analysis (organic solvents/free drug)
Excipient content analysis
Characterization
Liquid chromatography-mass spectrometry (LC-MS) analysis (intact/reduced molecular weight, sequence coverage, disulfide bond confirmation, and post-translational modification)
Liquid chromatography-mass spectrometry (LC-MS) analysis (ADC DAR value, ADC drug distribution, analysis on ADC linkage sites)
Molecular interaction(SPR/BLI)
Circular dichroism (CD), Differential scanning calorimetry (DSC)
Size exclusion chromatography - multi-angle light scattering (SEC-MALS) analysis, AUC
Micro-flow imaging (MFI)
Advantages
Comprehensive platform capabilities
Integrated platform solutions for quality research and analysis of monoclonal antibodies, bispecific antibodies, fusion proteins, ADCs, etc.
Pioneering advantage: Around 20 detection method platforms for tumor cell detection, providing report gene method testing
Ability to build detection cell lines for sample testing
ADCC/CDC testing platforms capabilities
Customized method development
Comprehensive platform-based solutions for quality research and analysis covering monoclonal antibodies, bispecific antibodies, fusion proteins, and ADCs, etc., with the capability to customize and optimize testing methods based on clients’ specific targets.
Further optimization and validation of analytical methods after method transfer from customer
Cutting-edge equipment and an elite team
Industry-leading instruments and equipment
Professional and experienced team, with core technical experts with 7 years of experience in average. Additionally, over 95% of the team members hold master’s degrees.
Workshop
The module is under construction
ADC R&D Service Request for Proposal
Name
*
Company Name
*
Tel
*
E-Mail
*
Sample Preparation Quantity
*
Conjugation Method
*
Cysteine-based site-specific conjugation
Enzyme-based site-specific glycoconjugation
Thiomab-based site-specific conjugation
ThioBridge-based site-specific conjugation
Sulfhydryl-based non-specific conjugation
Amino group based non-specific conjugation
Other alternative conjugation methods
DAR Value
*
DAR2
DAR4
DAR6
DAR8
Other specified DAR value
Large Molecular Type
*
Small Molecule Type
*
Estimated Demand Time
*
Your Specific Needs
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