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
Popular questions
Can Ceyone support impurity identification and characterization?
Yes. Analytical R&D can support the identification, characterization, and evaluation of impurities generated during pharmaceutical development and manufacturing.
Does Ceyone provide analytical method validation?
Yes. Ceyone supports analytical method validation activities to establish that analytical procedures are suitable, reliable, and reproducible for their intended purpose.
Can Analytical R&D support manufacturing and process development?
Yes. Ceyone’s Analytical R&D capabilities can support process development, scale-up, manufacturing, quality control, and other stages of the product development lifecycle.
What analytical R&D services does Ceyone provide?
Ceyone provides analytical development and testing support for pharmaceutical research and development programs, helping clients characterize compounds, monitor quality, and support development activities.
Can Ceyone develop analytical methods for new compounds?
Yes. Ceyone supports analytical method development and optimization for pharmaceutical compounds and intermediates, with methods designed to provide reliable and reproducible results.
What analytical techniques are available at Ceyone?
Ceyone’s analytical capabilities include techniques such as HPLC and GC, supported by laboratory infrastructure for characterization, testing, and quality evaluation.