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Integrated CDMO Services

From Discovery to Commercial, Accelerating Your Molecule to Market

CDMO Services

We provide integrated CDMO services covering the entire drug development lifecycle—from early discovery to commercial manufacturing. By combining advanced synthetic chemistry, scalable process development, robust analytical capabilities, and GMP-compliant production, we help partners accelerate the journey from molecule design to global market supply.

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Discovery

Our discovery services focus on enabling molecular innovation during the earliest stages of drug research. Through advanced synthetic chemistry and a diverse library of functional molecular building blocks, we help researchers rapidly explore novel chemical space and generate high-quality compounds for biological evaluation. This stage emphasizes creativity and feasibility exploration, supporting the discovery of new molecular structures for emerging therapeutic modalities such as targeted protein degradation, drug delivery ligands, and bioconjugation components.

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Process Development

Our process development platform transforms laboratory-scale chemistry into robust, scalable, and cost-effective manufacturing processes. Using advanced tools such as Design of Experiments (DoE), impurity profiling, and process modeling, we systematically optimize reaction conditions, improve yields, and enhance process robustness. Special expertise is applied to complex chemistries involved in bioconjugation linkers, radiopharmaceutical chelators, and heterocyclic or metal-containing compounds. The result is a well-characterized process ready for technology transfer, scale-up, and clinical or commercial manufacturing.

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Custom Synthesis

Our custom synthesis services deliver high-quality solutions for complex molecules, rare intermediates, and high-value compounds supporting modern pharmaceutical research and development. Backed by strong expertise in synthetic chemistry and scalable process design, we enable the efficient preparation of key components across multiple advanced therapeutic modalities, including drug delivery systems such as LNP and GalNAc, bioconjugation elements like ADC linkers, radiopharmaceutical chelators including DOTA and NOTA, and targeted protein degradation molecules such as PROTACs and molecular glues. In addition, we provide a diverse portfolio of functional molecular building blocks, covering heterocyclic compounds, nitrogen compounds, sulfur and selenium compounds, phosphorus compounds, metal complexes, and other specialized organic molecules, ensuring reliable access to critical materials that accelerate innovative drug discovery.

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Manufacturing

Our manufacturing capabilities support the reliable production of drug substances and key intermediates from clinical supply to commercial scale. Operating under stringent quality and regulatory standards, our facilities enable multi-step synthesis, handling of complex chemistries, and scalable production of advanced pharmaceutical materials. From kilogram-scale pilot production to large-scale manufacturing, we ensure consistent quality, secure supply chains, and efficient delivery of critical materials for pharmaceutical and biotech partners worldwide.

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Analytical Development

Our analytical development platform ensures product quality, process understanding, and regulatory compliance throughout the drug development lifecycle. We provide comprehensive analytical services including method development, method validation, impurity characterization, structural elucidation, stability studies, and release testing. Supported by advanced analytical technologies such as HPLC, LC-MS, NMR, and spectroscopy, our analytical teams deliver robust data packages that support process development, quality control, and global regulatory submissions.

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Services

CDMO Services

We provide integrated CDMO services covering the entire drug development lifecycle—from early discovery to commercial manufacturing. By combining advanced synthetic chemistry, scalable process development, robust analytical capabilities, and GMP-compliant production, we help partners accelerate the journey from molecule design to global market supply.

CDMO Services Overview

Discovery

Enabling Molecular Innovation at the Earliest Stages

Our discovery services focus on enabling molecular innovation during the earliest stages of drug research. Through advanced synthetic chemistry and a diverse library of functional molecular building blocks, we help researchers rapidly explore novel chemical space and generate high-quality compounds for biological evaluation. This stage emphasizes creativity and feasibility exploration, supporting the discovery of new molecular structures for emerging therapeutic modalities such as targeted protein degradation, drug delivery ligands, and bioconjugation components.

Key Capabilities

  • Synthetic Route Design - Design and screen efficient synthetic pathways using extensive building block resources and advanced synthetic chemistry expertise.
  • Custom Building Block Synthesis - Provide high-purity molecular fragments and key intermediates to support complex molecule construction.
  • Early Process Feasibility Assessment - Evaluate scalability, safety, and cost-effectiveness of synthetic routes at the early stage.
  • Research Sample Preparation - Deliver milligram- to gram-scale compounds for biological evaluation, pharmacokinetic studies, and toxicity testing.

Core Strengths

  • Expertise in challenging chemistries (fluorination, boron chemistry, hydrogenation)
  • Advanced platforms such as flow chemistry and biocatalysis
  • Experience across multiple therapeutic targets
Discovery

Process Development

Transforming Lab Chemistry into Scalable Manufacturing

Our process development platform transforms laboratory-scale chemistry into robust, scalable, and cost-effective manufacturing processes. Using advanced tools such as Design of Experiments (DoE), impurity profiling, and process modeling, we systematically optimize reaction conditions, improve yields, and enhance process robustness. Special expertise is applied to complex chemistries involved in bioconjugation linkers, radiopharmaceutical chelators, and heterocyclic or metal-containing compounds. The result is a well-characterized process ready for technology transfer, scale-up, and clinical or commercial manufacturing.

Service Scope

  • Process Optimization - Develop efficient, IP-friendly, and cost-competitive synthetic routes.
  • Process Characterization - Use Design of Experiments (DoE) to define critical process parameters and establish robust operating ranges.
  • Safety Evaluation - Conduct thermal risk analysis and calorimetric studies to ensure safe scale-up.
  • Impurity Profiling - Identify and control process-related impurities, including genotoxic impurities.
  • Technology Transfer - Enable smooth transfer of optimized processes to pilot or manufacturing facilities.

Value to Clients

  • Reduced development risks
  • Improved manufacturing efficiency
  • Faster progression to clinical supply
Process Development

Custom Synthesis

Flexible Solutions for Complex Molecules and High-Value Compounds

Our custom synthesis services deliver high-quality solutions for complex molecules, rare intermediates, and high-value compounds supporting modern pharmaceutical research and development. Backed by strong expertise in synthetic chemistry and scalable process design, we enable the efficient preparation of key components across multiple advanced therapeutic modalities, including drug delivery systems such as LNP and GalNAc, bioconjugation elements like ADC linkers, radiopharmaceutical chelators including DOTA and NOTA, and targeted protein degradation molecules such as PROTACs and molecular glues. In addition, we provide a diverse portfolio of functional molecular building blocks, covering heterocyclic compounds, nitrogen compounds, sulfur and selenium compounds, phosphorus compounds, metal complexes, and other specialized organic molecules, ensuring reliable access to critical materials that accelerate innovative drug discovery.

Service Workflow

  • Project Assessment - Clarify target structure, purity requirements, quantity, and delivery timeline.
  • Route Design - Develop customized synthetic pathways based on molecular complexity.
  • Lab-Scale Synthesis - Rapid laboratory synthesis and optimization to generate initial samples.
  • Scale-Up Production - Produce required quantities in kilogram laboratories or pilot plants.
  • Purification & Delivery - Apply crystallization, chromatography, or distillation to ensure product quality.

Reaction Expertise

  • Friedel-Crafts Reactions, Halogenation Reactions, Grignard Reactions
  • Coupling Reactions (e.g., Suzuki, Heck, Sonogashira)
  • Chiral Asymmetric Synthesis (e.g., Asymmetric Reduction, Alkylation)
  • Heterocyclic Compound Synthesis
Custom Synthesis

Manufacturing

Our manufacturing capabilities support the reliable production of drug substances and key intermediates from clinical supply to commercial scale. Operating under stringent quality and regulatory standards, our facilities enable multi-step synthesis, handling of complex chemistries, and scalable production of advanced pharmaceutical materials. From kilogram-scale pilot production to large-scale manufacturing, we ensure consistent quality, secure supply chains, and efficient delivery of critical materials for pharmaceutical and biotech partners worldwide.

Manufacturing Capabilities

  • GMP Production - Operate multi-purpose production facilities compliant with international GMP standards.
  • Scale-Up Production - Support production from kilogram scale to ton-level manufacturing.
  • Quality Assurance - Implement strict quality control covering raw materials, intermediates, and final products.
  • Process Validation - Conduct registration batches and Process Performance Qualification (PPQ).
  • Lifecycle Management - Continuous improvement and cost optimization for marketed products.

Key Advantages

  • Proven large-scale production capability
  • Global regulatory compliance
  • Flexible capacity and reliable delivery
Manufacturing

Analytical Development

Ensuring Quality, Process Understanding, and Regulatory Compliance

Our analytical development platform ensures product quality, process understanding, and regulatory compliance throughout the drug development lifecycle. We provide comprehensive analytical services including method development, method validation, impurity characterization, structural elucidation, stability studies, and release testing. Supported by advanced analytical technologies such as HPLC, LC-MS, NMR, and spectroscopy, our analytical teams deliver robust data packages that support process development, quality control, and global regulatory submissions.

Analytical Services

  • Method Development - Develop analytical methods for raw materials, intermediates, and APIs.
  • Method Validation - Validate analytical methods in accordance with ICH and GMP guidelines.
  • Impurity Identification - Characterize and quantify impurities using advanced analytical technologies.
  • Stability Studies - Conduct stability testing to support product shelf-life and regulatory filings.
  • Quality Documentation - Provide analytical data packages for CMC and regulatory submissions.

Analytical Technologies

  • HPLC / UPLC
  • GC / GC-MS
  • LC-MS / HRMS
  • NMR spectroscopy
  • Solid-state characterization
Analytical Development