From Scalable Preparative Chromatography to Rapid Analysis and Validation-Ready Methods
At Neopharm, we provide comprehensive services in chiral method development. Our team of experts specializes in chromatography-based techniques and can help you develop the most suitable separation procedure and conditions for your 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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Method Development and Validation Services in Chemistry
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Method Development and Validation Services in Microbiology
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Compatibility Studies Services
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Cleaning Validation Studies
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Filter Validation
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Chiral and Achiral Compounds Purification
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Experimental Polar Surface Area (EPSA)
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Disinfectant Efficacy Studies
We understand the intricate nature of chiral method development and the challenges that come with it, such as the need for enantiomeric resolution, increased selectivity, increased sensitivity, method robustness, and scalability. Our expertise, advanced technologies, and comprehensive approach ensure that your chiral method development endeavors yield accurate, reliable, and scalable results.
THE NEOPHARM SOLUTION
Achieve Optimal Results with Our Experienced Team
Our team can provide you with the right solutions for all your needs. From normal phase or supercritical fluid chromatography (SFC) for fast analysis and process monitoring; to reversed phase for bioanalysis.
We have you covered. All our methods are scalable for preparative chromatography use and analytical validation-ready for batch release and stability.
Get the Most Suitable Solution for Your Needs
We have extensive experience developing chiral methods that ensure optimal results with minimal effort. With our expertise, you can trust that your product will be analyzed quickly and efficiently while delivering the highest quality results.
Scalable Chiral Chromatography
We design our methods to be scalable, allowing you to use them for preparative chromatography when needed. This means faster analysis and process monitoring.
Validation-ready for Batch Release and Stability
Our methods are validation-ready, so you can be sure that your batches will be released on time and with the highest quality standards.
Normal Phase or SFC for Fast Analysis and Process Monitoring
Using our normal phase or SFC methods, you can get results quickly while ensuring the accuracy and precision of your data.
Neopharm Answers to Common Questions about Chiral Method Development:
Chiral method development involves the creation of analytical methods to separate chiral compounds into their individual enantiomers. It encompasses the optimization of chromatographic conditions, selection of appropriate columns, mobile phases, and detection techniques to achieve effective resolution.
Chiral compounds play a significant role in the pharmaceutical industry. Developing accurate and reliable methods for chiral separation is crucial for drug development, quality control, and regulatory compliance. It ensures the assessment of enantiomeric purity, determination of chiral impurities, and characterization of pharmacokinetics.
Neopharm employs a comprehensive approach to chiral method development, combining our expertise, state-of-the-art technology, and customized solutions. We carefully assess the compound characteristics, project goals, and regulatory requirements to design and optimize chiral separation methods that deliver precise and reproducible results.
By choosing Neopharm, you benefit from our specialized expertise in chiral separations, our state-of-the-art technology, and our commitment to tailored solutions. Our developed methods offer enhanced selectivity, sensitivity, and robustness. We ensure compliance with regulatory guidelines, providing you with accurate and validated methods for your specific chiral compounds.
Chiral method development involves the creation of analytical methods to separate chiral compounds into their individual enantiomers. It encompasses the optimization of chromatographic conditions, selection of appropriate columns, mobile phases, and detection techniques to achieve effective resolution.
Chiral compounds play a significant role in the pharmaceutical industry. Developing accurate and reliable methods for chiral separation is crucial for drug development, quality control, and regulatory compliance. It ensures the assessment of enantiomeric purity, determination of chiral impurities, and characterization of pharmacokinetics.
Neopharm employs a comprehensive approach to chiral method development, combining our expertise, state-of-the-art technology, and customized solutions. We carefully assess the compound characteristics, project goals, and regulatory requirements to design and optimize chiral separation methods that deliver precise and reproducible results.
By choosing Neopharm, you benefit from our specialized expertise in chiral separations, our state-of-the-art technology, and our commitment to tailored solutions. Our developed methods offer enhanced selectivity, sensitivity, and robustness. We ensure compliance with regulatory guidelines, providing you with accurate and validated methods for your specific chiral compounds.
Partner with Neopharm today to take advantage of our expertise, advanced technology, and tailored solutions for accurate and reliable Chiral Method Development. Contact us now to discuss your specific requirements.
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