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Pharmaceutical Chemistry & Quality Assurance Research
- Analytical method development and validation
- Bioanalytical method development and Validation
- Impurity Profiling • Standardization and analysis of herbal formulation
- Formulation and development of herbal drugs
- Stability indicating assay method development and validation of pharmaceuticals and their combined dosage form
- Dissolution studies
- Stability studies of active pharmaceutical ingredients and dosage forms as per ICH guidelines
- Forced degradation studies (Stress conditions) and accelerated stability conditions of API and combined dosage forms
- Drug Design
- Synthesis of heterocyclic molecules
- Computational chemistry
- Process development and optimization
