Maximum precision in Residual solvents analysis

Neopharm offers exceptional analytical services that can detect even the slightest traces of residual solvents using GCand gravimetric methods. Their results are of the highest quality and meet industry standards, and they offer customizable services that cater to your specific needs.

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We have services to speed up your product development.

We provide reliable GMP quality control testing and innovative R&D solutions to accelerate product development and improve people's lives.

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Compliance with regulatory guidelines and limits for residual solvents is essential, and failure to meet these standards can result in product recalls, fines, and damage to your reputation.

THE NEOPHARM SOLUTION

Accurate results you can trust

Our advanced chromatographic techniques provide accurate and reliable results that meet the highest standards of quality.  

Rely on our expertise

We have a team of experienced professionals who are highly skilled at testing residual solvents. We also conduct rigorous quality control tests to ensure accuracy and precision in every sample we analyze.

Comprehensive Methodology 

Our experienced team of chemists follows strict quality control measures and adheres to regulatory guidelines, ensuring the accuracy and precision of our analysis. We can also validate any method to ensure reliable and reproducible results.

Neopharm Answers to Common Questions about Residual Solvents Analysis

Residual solvents are volatile organic compounds that may remain following synthesis of the drug substance or manufacturing of the drug product. They can pose health risks and must be controlled within permissible limits.

Residual solvents analysis is crucial to ensure the safety and quality of pharmaceuticals, nutraceuticals, and other products. It helps identify and quantify the presence of potentially harmful solvents, ensuring compliance with regulatory guidelines and protecting consumer health.

Our residual solvents analysis primarily employs Gas Chromatography (GC), a highly sensitive and selective technique that allows for accurate detection and quantification of residual solvents in a wide range of samples.

Regulatory limits for residual solvents vary depending on the specific product and regulatory authorities. Our team is well-versed in these limits and can guide you in determining the applicable standards for your industry and region.

The turnaround time for residual solvents analysis depends on the specific requirements of your project and the complexity of the samples. We strive to provide results within a reasonable timeframe, ensuring efficient and prompt service.

Ensure the purity and safety of your products with Neopharm's Residual Solvents Analysis. Contact us today to discuss your specific needs and experience the accuracy and reliability of our advanced analytical services. 

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