Is your product pure enough?
Comprehensive purity analysis and quality verification
Ensure your products meet the highest quality standards with our precise purity analysis and comprehensive quality assessment services.
Precision Purity Analysis
Our comprehensive approach combines multiple analytical techniques to provide accurate purity determination and complete quality characterization of your materials.
Accurate purity determination with validated methods
Comprehensive impurity profiling and identification
Regulatory compliance support (USP, EP, ICH guidelines)
Certificate of Analysis with full traceability
Quality assurance for critical materials
Batch-to-batch consistency verification
Support for supplier qualification programs
Expert consultation on quality specifications
Advanced Purity Analysis Techniques
We utilize state-of-the-art analytical methods to deliver precise purity measurements and comprehensive quality assessment.
NMR Spectroscopy
Quantitative purity analysis with high precision, typically achieving ±0.1% accuracy.
LC-MS Analysis
Comprehensive impurity profiling and identification of unknown contaminants.
Thermogravimetric Analysis
Determines organic content, moisture, and residual solvent levels.
ICP-MS
Ultra-sensitive detection of trace metals and elemental impurities.
HPLC Analysis
Precise quantification of main components and related substances.
Karl Fischer Titration
Accurate water content determination for moisture-sensitive materials.
Quality Assessment Workflow
Our systematic approach ensures accurate and reliable purity analysis with full regulatory compliance.
Purity Requirements
Define target specifications and acceptance criteria.
Method Selection
Choose optimal analytical techniques for your specific material.
Quantitative Analysis
Precise measurement using validated analytical methods.
Quality Certification
Comprehensive certificate of analysis with regulatory compliance.
Quality Success Stories
API Purity Verification
Desafio:
A pharmaceutical company needed to verify the purity of their active pharmaceutical ingredient (API) to meet FDA requirements for drug registration.
Solução:
We performed quantitative NMR analysis for overall purity determination, LC-MS for impurity profiling, and ICP-MS for elemental impurities according to ICH Q3D guidelines.
Resultado:
Confirmed API purity at 99.8% with full impurity characterization, enabling successful regulatory submission and product approval.
Raw Material Qualification
Desafio:
A specialty chemical manufacturer needed to qualify a new supplier for a critical raw material used in high-performance coatings.
Solução:
Comprehensive purity assessment using HPLC for main component quantification, TGA for moisture and volatile content, and LC-MS for impurity identification.
Resultado:
Successfully qualified the new supplier with detailed material specifications, resulting in 20% cost reduction while maintaining product quality.
Need Purity Analysis?
Ensure your products meet quality standards with our expert purity analysis services. Get accurate results you can trust.