Advanced NMR, MS, and IR analysis to reveal complex molecular structures.
We provide comprehensive impurity identification and quantification services to ensure the safety and efficacy of pharmaceutical products. Our advanced analytical techniques deliver precise and reliable results.
Utilizing HPLC, UPLC, and GC to separate and quantify impurities with high precision. Employing LC-MS/MS and GC-MS for accurate identification and quantification of impurities. Using NMR and UV-Vis spectroscopy for additional structural information and quantification.
At ARSI Canada, we specialize in structure elucidation and characterization to accelerate drug discovery and development. Using advanced techniques like mass spectrometry, NMR spectroscopy, and X-ray crystallography, our experienced team can precisely identify and confirm the chemical structures of small molecules. This allows for a detailed understanding of a compound’s biological activity, target specificity, and potential interactions with other molecules, ensuring your research is on the right track.
Our comprehensive structure elucidation services provide critical insights into the physicochemical properties of compounds, including solubility, stability, and bioavailability, which are essential for optimizing drug formulations. Whether you’re in the early stages of drug discovery or optimizing lead compounds, ARSI Canada delivers high-quality data and detailed reporting to help you move forward with confidence.
Provides detailed information about the molecular structure of impurities. Offers high-resolution mass data to aid in the elucidation of molecular structures. Determines the three-dimensional structure of crystalline impurities. Used for complementary structural information and confirmation of impurity structures.
We conduct degradation studies to understand the stability of drug substances and products, identifying potential degradation products and their impact.
Exposing drug substances to stress conditions (heat, light, pH, etc.) to identify degradation products. Developing and validating methods to monitor impurities over the product’s shelf-life.
With expertise in custom synthesis, analytical services, and drug development.
We are here to support all your research needs by reducing the project timeline and cost.
Impurity Identification and Quantification
Chromatographic Techniques
Mass Spectrometry
Spectroscopic Techniques
Structure Elucidation
NMR Spectroscopy
Mass Spectrometry
X-Ray Crystallography
FTIR and Raman Spectroscopy
Degradation Studies
Stress Testing
Stability-Indicating Methods
We clarify targets, specs, safety, and timelines; align on success criteria and CDA/IP terms.
Route scouting, risks, and costed plan with deliverables, data package, and milestones.
Synthesis, in-process controls, purification, and analytical verification at each stage.
Materials shipped per spec with full documentation and optional tech transfer support.
Share your target, quantity, and timeline — we’ll return a clear, cost-effective proposal.
We operate with rigorous QC, data integrity, and traceability aligned with international guidelines. Every shipment includes complete analytical documentation and batch records.
Explore our range of specialized solutions designed to support your unique needs with quality, reliability, and expertise.
