Services - Therapeutic Proteins & Peptides

One-stop Solution for Therapeutic Proteins & Peptides

Collaborate with our expert team on projects covering the entire proteins and peptides development, including therapeutic proteins and peptides discovery and process development, pre-formulation studies, formulation development, CGMP manufacturing, etc.

Let CD Formulation be your partner in proteins and peptides development, and we will work together to promote the development of the field of biologics.

Therapeutic Proteins Production

CD Formulation provides comprehensive therapeutic protein and peptide characterization services, including but not limited to protein and peptide structural characterization, quantitative analysis, peptide map analysis, sequencing analysis, post-translational modification analysis, thermal denaturation analysis, crystallization analysis, and druggability evaluation, etc.

Therapeutic Peptides Production

CD Formulation has a series of facilities that comply with current good manufacturing practice (cGMP) requirements and is committed to providing you with total solutions for therapeutic protein and peptide CGMP manufacturing, including cGMP therapeutic protein and peptide manufacturing and formulation cGMP Manufacturing.

Therapeutic Proteins & Peptides Process Development

CD Formulation supports one-stop development services from upstream to downstream bioprocessing, including cell line development and cell culture, upstream process development, downstream process development, process characterization and process validation, and process transfer, etc., to ensure your products comply with regulatory approvals.

Therapeutic Proteins & Peptides Drug Delivery System Development

CD Formulation's expert team can design and develop the best delivery method for you based on your product's application field and route of administration, including but not limited to oral formulation, transdermal formulation, injections, pulmonary formulation, intranasal formulation, and a series of innovative drug delivery routes.

Therapeutic Protein& Peptide Characterization

CD Formulation provides comprehensive therapeutic protein and peptide characterization services, including but not limited to protein & peptide structural characterization, protein advanced structure characterization, quantitative analysis, peptide map analysis, sequencing analysis, amino acid analysis, post-translational modification analysis, thermal denaturation analysis, Crystallization analysis, and druggability evaluation, etc.

cGMP Manufacturing

CD Formulation has a series of facilities that comply with current good manufacturing practice (cGMP) requirements and is committed to providing you with total solutions for therapeutic protein & peptide CGMP manufacturing, including cGMP therapeutic protein & peptide manufacturing and formulation cGMP Manufacturing.

Supporting Analysis Services for Protein & Peptide Formulation Development

With deep expertise in protein & peptide formulation development, CD Formulation uses advanced analytical methods to support the characterization of therapeutic proteins/peptides, stabilizing excipients, packaging materials, and protein/peptide formulations. Our biopharmaceutical analytical laboratory continuously updates and improves analytical methods to ensure optimal results and the highest quality standards. Whether you are in the early stages of development or about to submit a listing application, CD Formulation's professional team can provide customized solutions based on your specific needs.

Therapeutic Proteins & Peptides Characterization

Structural Characterization
Higher-Order Protein Structures Characterization
Peptide Mapping Analysis
Particle and Aggregation State Characterization
Viscosity Analysis
Quantitative Analysis
Sequencing Analysis
Amino Acid Analysis
Post-translational Modification Analysis
Stability and Thermal Denaturation Analysis
Crystallization Analysis
Druggability Assessment
...

Quality Control Testing

Analytical Method Development and Validation
Analytical Method Transfer
Product-related Impurity
Process-related Impurity
Elemental-related Impurity
Residual Solvent and Volatile Impurity
Extractables and Leachables
Biosimilarity Study
Comparability Study
Stability Testing
Batch-release Testing
Forced Degradation Study
...

Laboratory Equipment Highlights

Dynamic Light Scattering (DLS) Analysis
Differential Scanning Fluorescence (DSF) Analysis
Protein Chip Bioanalysis
Differential Scanning Calorimetry (DSC) Analysis
Spectral Analysis
Chromatography Analysis
Nanoparticle Tracking Analysis
Bioanalyzer
...

Why Choose CD Formulation?

Expert in complex therapeutic proteins/peptides development and characterization, ensuring close monitoring of proteins/peptides throughout process development for scale-up.
Comprehensive knowledge, insights, and expertise in therapeutic protein/peptide formulation development, process development, analytical development, quality, and GMP manufacturing.
Extensive experience in multiple therapeutic proteins/peptides drug delivery routes, including but not limited to oral, injection, microneedle, nano delivery, etc.
Flexible transfer capabilities for process development of therapeutic protein/peptide and its formulation.
End-to-end workflow from preformulation studies to commercial cGMP manufacturing.
Collaboration of multiple analytical testing services to save your time in your drug development.
The coordinated execution of multiple analytical testing services ensures time savings for the launch of your commercial proteins/peptides products.