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. Tell us your throughput, sample type and compliance requirement and we will send the full datasheet for the right model.
Request the datasheetCompliance & 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.
Company catalogs
Our full range, supplied, installed and serviced in Bangladesh by our own Technical Services Division.
- Innovation in Laboratory Solutions (PDF, opens in a new tab) The full range: instrumentation and process systems, spectroscopy, environmental and stability systems, pharmaceutical testing, laboratory infrastructure, safety cabinets, standards and the digital QC platforms.
- Food & Dairy Quality Control Solutions (PDF, opens in a new tab) The food and dairy laboratory: cryoscopy, Gerber fat analysis, rapid test kits, measurement and monitoring, controlled-temperature storage and LIMS.
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.