Solutions for Active Pharmaceutical Ingredients
Active pharmaceutical ingredient (API), is the term used to refer to the biologically active component of a drug product (e.g. tablet, capsule). API is the primary ingredient in the Drug products which is usually composed of several other components.
Thermofisher Scientific offers innovative solutions at every stage of the API manufacturing process through our unmatched range of advanced analytical technologies, lab equipment, chemicals, consumables, software, and services.
R&D
- Confidence in result
- Sensitivity
QC
- High throughput
- QbD
Manufacturing
- Cost optimization
- Right first time
Compliance
- cGLP/ cGMP
- Data integrity
- Validation
Effluent Treatment
- Regulatory changes
- Online monitoring
- Genotoxic impurity profiling (NDMA)
Genotoxic impurities in pharmaceuticals are of increasing concern and hence determination of potential genotoxic impurities plays a key role. Our range of high purity LCMS solvents to assist your analysis for reliable results. - Heavy Metal Analysis
We offer high purity Acids Optima and Trace metal along with ICP standards required for the heavy metals test in detection and estimation of the metallic impurities of active pharmaceutics ingredients as per USP <232> <233> - Residual Solvent Analysis - GCHS
Identification and quantification of Residual solvent and organic volatile impurities in active pharmaceutical ingredients by GC. You can rely on our GC HS solvents. - Impurity Profiling
Explore our range of Chromatography solvents and reagents which are readily available to serve you faster - Moisture Estimation
Our Karl Fischer reagents portfolio is designed to meet the needs of the analytical chemist by providing accurate moisture content determination using volumetric & Coulometric titration with unique benefits.
