Gas Chromatography

Gas Chromatography (GC) is a cornerstone of our analytical capabilities, used to separate and analyze volatile and semi-volatile compounds in pharmaceutical samples. This technology ensures precise identification and quantification of components in complex mixtures, which is essential for verifying the purity and consistency of drug formulations and excipients. With its high sensitivity and reproducibility, GC plays a critical role in maintaining product integrity and supporting regulatory compliance in pharmaceutical manufacturing.

Atomic Absorption Spectroscopy

Atomic Absorption Spectroscopy (AAS) is an essential tool for detecting and quantifying trace metals in pharmaceutical raw materials and finished products. Trace metals, even in minute amounts, can affect the safety and efficacy of drugs, making their detection vital for compliance with regulatory standards. Our AAS setup ensures highly accurate and reliable results, supporting manufacturers in maintaining the quality and safety of their products while adhering to stringent global guidelines.

Fourier Transform Infrared Spectroscopy

Fourier Transform Infrared Spectroscopy (FTIR) is a versatile instrument used to identify and characterize the chemical composition of pharmaceutical materials. By analyzing the unique molecular fingerprints of substances, FTIR ensures the quality and authenticity of raw materials, excipients, and drug formulations. This instrument is indispensable for method validation and quality assurance, helping to maintain consistency across all stages of pharmaceutical production while meeting international standards.

Ultraviolet-Visible Spectroscopy

Ultraviolet-Visible Spectroscopy (UV) is a reliable method for quantitative analysis of pharmaceutical samples, used extensively for measuring absorbance and concentration levels. This instrument supports the accurate determination of active ingredients and impurities in drug formulations, ensuring compliance with quality and regulatory requirements. Its applications include routine quality control, stability testing, and formulation development, making it a vital part of our analytical processes.