Instruments

LC-MS

Mass Spectrometry (MS) is a powerful analytical technique used to identify and quantify molecules based on their mass-to-charge ratio.

It plays a pivotal role in various scientific disciplines, ranging from pharmaceuticals and biotechnology to environmental analysis and forensics.

MS allows us to gain unprecedented insights into complex mixtures, elucidate molecular structures, and detect trace-level components with exceptional precision, ultra-high sensitivity, speed, high resolution mass accuracy, expanded compound coverage, robust performance and reliability.

UHPLC

UHPLC is a state-of-the-art analytical technique that builds upon traditional High-Performance Liquid Chromatography (HPLC) but takes it to a whole new level.

This method allows for superior separation and quantification of complex mixtures with unparalleled speed, sensitivity, versatility and efficiency.

It is a cornerstone technology in modern analytical laboratories due to its ability to handle challenging samples, making it an indispensable tool across diverse industries

GC-MS

Gas Chromatography-Mass Spectrometry (GC-MS) is a powerful analytical technique that combines the separation capabilities of Gas Chromatography (GC) with the identification and quantification abilities of Mass Spectrometry (MS).

It is a versatile and widely used method for analysing complex mixtures, enabling the detection and characterization of volatile and semi-volatile compounds with high sensitivity and specificity. Precision is paramount, GC-MS enables us to delve into complex mixtures, accurately identifying target compounds at trace levels.

By leveraging its robust chromatographic separation and mass spectral fragmentation patterns and gain a comprehensive understanding of chemical structures, isomers, and impurities. This level of detail is critical in characterizing potential drug candidates and ensuring the highest standards of pharmaceutical quality.

ICP-MS

The integration of ICP-MS into our laboratory workflows empowers us to explore the elemental composition of pharmaceutical formulations, raw materials, and biological samples at trace levels, providing critical insights into the safety, efficacy, and quality of products with its exceptional sensitivity and precision.

ICP-MS plays a vital role in pharmacokinetic studies, allowing us to trace the distribution of elements in biological samples and assess drug bioavailability.

By accurately quantifying trace elements in tissues and body fluids, we gain insights into drug metabolism, tissue distribution and excretion, aiding in the design of effective and safe medications.

This technology broadens our understanding of pharmaceutical formulations and guides the development of advanced drug products.

Dissolution System

To ensure the highest quality and efficacy of drug formulations, we are proud to incorporate Dissolution Systems into our analytical capabilities.

Dissolution process plays a vital role in predicting drug release and bioavailability, enabling us to optimize formulation parameters and ensure that our medications perform as intended in the human body.

Dissolution Systems are built to adhere to global guidelines and standards, ensuring that our dissolution testing aligns with industry best practices. This compliance helps us confidently demonstrate the quality and consistency of formulations during the drug approval process.

The precise control over experimental parameters and automated sampling capabilities enable us to generate reliable data efficiently, expediting decision-making and optimizing formulation strategies.

LC-MS

Mass Spectrometry (MS) is a powerful analytical technique used to identify and quantify molecules based on their mass-to-charge ratio.

It plays a pivotal role in various scientific disciplines, ranging from pharmaceuticals and biotechnology to environmental analysis and forensics.

MS allows us to gain unprecedented insights into complex mixtures, elucidate molecular structures, and detect trace-level components with exceptional precision, ultra-high sensitivity, speed, high resolution mass accuracy, expanded compound coverage, robust performance and reliability.

UHPLC

UHPLC is a state-of-the-art analytical technique that builds upon traditional High-Performance Liquid Chromatography (HPLC) but takes it to a whole new level.

This method allows for superior separation and quantification of complex mixtures with unparalleled speed, sensitivity, versatility and efficiency.

It is a cornerstone technology in modern analytical laboratories due to its ability to handle challenging samples, making it an indispensable tool across diverse industries

GC-MS

Gas Chromatography-Mass Spectrometry (GC-MS) is a powerful analytical technique that combines the separation capabilities of Gas Chromatography (GC) with the identification and quantification abilities of Mass Spectrometry (MS).

It is a versatile and widely used method for analysing complex mixtures, enabling the detection and characterization of volatile and semi-volatile compounds with high sensitivity and specificity. Precision is paramount, GC-MS enables us to delve into complex mixtures, accurately identifying target compounds at trace levels.

By leveraging its robust chromatographic separation and mass spectral fragmentation patterns and gain a comprehensive understanding of chemical structures, isomers, and impurities. This level of detail is critical in characterizing potential drug candidates and ensuring the highest standards of pharmaceutical quality.

ICP-MS

The integration of ICP-MS into our laboratory workflows empowers us to explore the elemental composition of pharmaceutical formulations, raw materials, and biological samples at trace levels, providing critical insights into the safety, efficacy, and quality of products with its exceptional sensitivity and precision.

ICP-MS plays a vital role in pharmacokinetic studies, allowing us to trace the distribution of elements in biological samples and assess drug bioavailability.

By accurately quantifying trace elements in tissues and body fluids, we gain insights into drug metabolism, tissue distribution and excretion, aiding in the design of effective and safe medications.

Dissolution System

To ensure the highest quality and efficacy of drug formulations, we are proud to incorporate Dissolution Systems into our analytical capabilities.

Dissolution process plays a vital role in predicting drug release and bioavailability, enabling us to optimize formulation parameters and ensure that our medications perform as intended in the human body.

Dissolution Systems are built to adhere to global guidelines and standards, ensuring that our dissolution testing aligns with industry best practices. This compliance helps us confidently demonstrate the quality and consistency of formulations during the drug approval process.

The precise control over experimental parameters and automated sampling capabilities enable us to generate reliable data efficiently, expediting decision-making and optimizing formulation strategies.