Analytical Chemistry

Analytical chemistry department is well equipped with state-of-the-art instrumentations and experienced chemists for performing chemical characterization for agrochemicals, pharmaceutical and other industries. We can analyze all types of molecules as per the relevant national / international guidelines such as OECD, BIS, OPPTS, EPA, EU, ASTM, EEC, FDA, IP, USP, ICH, ABNT NBR, SANCO and WHO etc. From a regulatory perspective, scientific insight and experimental rigor to GLP standards are essential to generate first-hand experimental data using appropriate methods with high levels of accuracy and reproducibility.

• Method development and method validation

For all regulatory submissions, validation of an analytical method is essential to ensure the accuracy, precision, specificity, LOD, LOQ, linearity & range and robustness of data being collected.

• Chemical characterization (ATR – Analytical test report)
• Impurity profiling and 5 batch analysis

While generating the product specifications for global regulatory submissions, 5-batch analysis is essential for the registration of agrochemicals that is required to prove their chemical equivalence.

• Physical and chemical properties of technical and formulation grade
• Storage stability
  • Accelerated storage studies
  • Cold temperature storage stabilities
  • Long-term storage stability & corrosion characteristics studies (1-2 Years)
  • Stability at shelf life (storage stability)- one year/2-year/cold temp.
  • Storage stability with metal and metal ion at normal and elevated temperature
• Dose formulation analysis (For toxicity studies)
• Elemental analysis

Identification and quantification of elemental / metal composition in diversified sample types

• Pharmaceuticals
• Agrochemical technical materials and other chemicals
• Soils, sediments, etc.
• Processed food & feed
• Nutraceuticals
• Biological matrices, like tissues, blood / plasma, etc.
• Water
• Leachable and extractable analysis for medical devices