Our Analytical R&D service combines advanced instrumentation, scientific rigor, and collaborative workflows to support drug discovery, development, and quality control. Our expert analytical team works closely with chemists and process scientists to design, validate, and apply methods that ensure your compounds are characterized, pure, stable, and compliant.
- Method Development & Optimization
We design tailored analytical methods (HPLC, UPLC, GC, etc.) optimized for sensitivity, accuracy, and robustness to suit each stage of your project.
- Compound Characterization
Using tools like NMR (1H, 13C, 2D methods), MS, IR, UV-Vis, and others, we fully characterize molecular structure, purity, and other physical/chemical properties.
- Impurity Profiling & Forced Degradation
Detecting, quantifying, and understanding impurities (known and unknown), including stressed condition studies to assess stability and degradation pathways.
- Purification & Isolation
Preparing pure compounds via prep-HPLC (normal & reverse phase), lyophilization, crystallization, and other isolation techniques to prepare standards, intermediates, or batch materials.
- Stability Studies
Evaluating compound stability under various environmental and storage conditions to support shelf life, formulations, and regulatory requirements.
- Regulatory-Grade Documentation & Support
Ensuring analytical methods and results meet global regulatory standards; aiding in method validation, transfer, reference standard qualification, and reporting.
Why Choose Ceyone for Analytical R&D?
Integrated workflows: analytical work tightly aligned with synthetic, medicinal chemistry, process and quality teams
Flexible scale: from small discovery-scale analysis to regulatory and commercial support
High precision & reproducibility: validated methods, thorough documentation, and robust quality systems
Accelerated timelines: experienced analysts, modern instrumentation, and efficient project hand-offs