Contract Analytical Development
API Method Verification/Validation
Accurate API verification/validation ensuring compliance with regulatory standards and product quality.
Raw Material Analysis/ Verification/ Validation
Comprehensive raw material testing ensuring compliance with industry standards.
Finished Product Method Development
Innovative method development for precise analysis of finished products.
Finished Product Method Validation
Rigorous validation of analytical methods for reliable finished product quality assessment.
Stability Studies
Long-term and accelerated stability testing to ensure product shelf life and safety.
ELSD
Evaporative light scattering detection for non-volatile compound analysis with high sensitivity.
RI
Refractive index analysis for identification and quality control of pharmaceutical formulations.
Fluorescence
Fluorescence analysis to determine trace quantities and sensitive detection in pharmaceutical products.
Arsenic Test
Specialized arsenic testing ensuring elemental impurities are within safe limits.
Freezing Point
Determination of freezing point for stability characterization of liquid formulations.
Particulate Morphology
Analysis of particulate morphology to understand shape, size, and distribution for formulation quality.
Size, Shape, Surface Area of Individual Particle
Comprehensive particle analysis for optimal drug dispersion and stability.
Extractable & Leachable
Analysis of container components to ensure product safety from potential extractables and leachables.
Synthesis & Characterization of Unknown Impurities
Identification, synthesis, and characterization of unknown impurities for safety assessment.
Polymer Synthesis
Custom polymer synthesis for enhanced drug delivery systems and controlled release formulations.
Ethylene Oxide
Analysis of ethylene oxide residues to ensure safety and regulatory compliance.
Hydroxyl Value Analysis
Hydroxyl value determination to evaluate raw material suitability for formulation processes.
IVRT
In-vitro release testing to evaluate drug release rates for topical and transdermal products.
Rheology
Rheological studies to characterize viscosity and flow properties of formulations.
Particle Size Analysis
Accurate particle size distribution analysis for optimal product stability and bioavailability.
Nitrosamine
Testing for nitrosamine impurities to ensure product safety and regulatory compliance.
Elemental Impurities
Elemental impurity testing to meet ICH guidelines and ensure patient safety.
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