Delivering high quality analytical services
We provide all-inclusive analytical solutions including method development, method validation, method transfer, characterization studies, batch release & stability analysis. We are specialized in developing high challenging analytical methods for API, Formulations, combi-chem library molecules.
For process development and stability testing, we support with approaches like, analytical methods development combined with in-house validation, Transferring developed methods to the client. Additionally, we also offer our expertise in semi-preparatory to preparatory purification, impurity isolation, structural elucidation, and characterization.
Marking our role as vital for clients from discovery to development processes of pharmaceuticals, fine chemicals, agrochemicals, and other products.
Ensuring the benchmarks of analytical service with rapid turn-around time.
Offering cGMP & GLP compliant services for Drugs and Pharma:
Services we offer
- Analytical Method Development
- Method Verification/Validation
- Structural Characterization and Elucidation
- Reference & Working Standards Qualification
- Identification & Characterization of Impurities and Unknown Impurities
- Structure Elucidation & Structural Characterization of degradants and metabolites
- Elemental Impurity Analysis by ICPMS( Screening, Validation, Batch Analysis)
- Stability, Solubility, Dissolution
- Mapping and Imaging Studies
- Routine purification
- Chiral separation
- Thermal analysis
- Particle Size Determination (PSD) services: shape and crystallinity determination
- Thermal Analysis and Calorimetry
- Unknown Particulate Identification
- Solid-State Chemistry and Particle Engineering
- Polymorphism (pXRD)
- Extractables and Leachables
- Batch Release and Stability Lot Testing
- Carryover studies
- Force Degradation Studies
- Impurity Isolations and Identification
- Genotoxic Impurity Studies
- Drug/Excipient Interaction Studies
Looking for a specialized analytical service? Let’s Talk