Analytical & Impurity Standards
Characterised impurity and degradation-product standards for method development.
Characterised impurity, degradation product and related-substance standards, supplied with structural confirmation and assigned purity. Without them a related-substances method cannot be validated for specificity, and an unknown peak stays unknown.
- Import, delivery and installation
- IQ/OQ and calibration by our Technical Services Division
- Genuine spares and operator training in Dhaka
Specifications
Specifications vary by model and configuration — the brochure carries the full range. Tell us your throughput, sample type and compliance requirement and we will confirm which model fits.
Download the brochure (PDF · 4 KB)Compliance & qualification
Impurity control per ICH Q3A and Q3B; mutagenic impurities per ICH M7.
Applications
Related substances methods, forced degradation and stability-indicating method development, specificity validation, genotoxic impurity work.
Also in Pharmaceutical Standards & Specialty Chemicals
Related products
Secondary & Working Standards
Standards qualified against a primary reference for routine analytical use.
Active Pharmaceutical Ingredients (APIs)
Bulk active substances from certified manufacturers, supplied against specification.
Drug Intermediates
Intermediate compounds used in the synthesis of active substances.