Analytical Services
From characterization to stability studies, impurity profiling, compatibility testing, and method validation, our analytical services help clients achieve reliable results throughout the entire product development lifecycle.
Analytical R&D Service Capabilities
- API characterization
- Polymorphism studies
- Protein purification & characterization
- Analysis of primary glassware
- Solubility studies
- Log P and Log D determination
- Diluent compatibility studies
- Method development with all detector types
- Analytical method validation
- Analytical method transfer
- Analytical methods for cleaning verification & validation
- IVRT method development & validation
- IVPT method development & validation
- API, excipient, and drug-product compatibility studies
- Photostability studies
- Freeze–thaw stability studies
- Stability studies as per ICH zones
- Forced degradation studies
- Leachable & extractable studies
- Glass delamination studies
- Genotoxic impurities analysis
- Reverse engineering
- Dissolution studies as per BPC
Which industries do you support?
We support pharmaceutical, food, FMCG, environmental testing, and oil & gas sectors with advanced analytical solutions.
Do you perform method development for all types of detectors?
Yes, we develop analytical methods for UV, PDA, RI, ELSD, FID, CAD, MS, and other detectors.
Can you handle unstable or highly complex drug molecules?
Yes, we have strong expertise in managing sensitive, thermolabile, and complex drug substances.
Do you provide stability studies?
Yes, we conduct stability studies as per ICH guidelines, including photostability, freeze–thaw, and forced degradation studies.
Are compatibility studies included?
Yes, we perform API–excipient, drug-product, and diluent compatibility studies.
Do you offer impurity profiling and GTI analysis?
Yes, we provide test methods for genotoxic impurities, process impurities, and degradation profiling.
Is cleaning method validation available?
Yes, we develop and validate cleaning verification methods as per regulatory guidelines.
Can you support method validation and transfer?
Yes, we offer complete method validation and method transfer services.
Do you conduct dissolution and performance testing?
Yes, dissolution studies as per BPC and performance testing for specific dosage forms are available.
How can we request analytical services?
Services can be requested via call, email, or online inquiry, and our team will schedule support based on project requirements.