Accuracy in Chromatography Solutions for Drug Development

At Neopharm, we understand our customers' challenges during drug development, particularly in chromatography services. We work closely with our clients to develop solutions to help their pharmaceutical research, drug discovery, and quality control.

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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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Our expertise in selecting the most suitable chromatography technique and our specialized knowledge and capabilities allow us to determine the most appropriate method to support your projects. 

We prioritize providing efficient and cost-effective services to help our customers navigate constraints in drug development timelines.

Our Services

Chiral Separation

The enantiomeric purity of drugs can significantly impact their efficacy and safety. At Neopharm, we specialize in chiral separation techniques to ensure the accurate resolution of enantiomers, providing tailored solutions to meet your specific needs.

Analytical Method Development and Validation

Our experienced team specializes in developing and validating analytical methods to ensure accurate and reproducible results. Whether you need assay development, screening, or method optimization, we have the expertise to meet your requirements.

Chromatography-Based Purification

We offer chromatography-based purification services for isolating compounds, including chiral separation and compound library screening. Our purification methods are customizable to your specific needs, ensuring high purity and yield.

HPLC Analysis and Method Development

With state-of-the-art HPLC instrumentation and expertise, we provide comprehensive analysis and method development services. From stability indicating methods to gradient method development, we deliver precise and efficient solutions.

Assay Development and Screening

Accelerate your drug discovery process with our assay development and screening services. Our assays are tailored to target-specific requirements, providing valuable insights into compound activity and potency.

Custom Pre-formulation Services

We offer custom pre-formulation services to support early-stage drug development. From physicochemical analysis to stability indicating assays, we help optimize formulations for efficacy and stability.

The Neopharm Solution

Expertise: Our team of experienced chromatography scientists specializes in method development, ensuring optimized separation, detection, and quantification of target compounds. We navigate the complexities of analytical techniques, providing solutions tailored to your specific requirements.

Reliability: We adhere to strict quality standards and ensure the reliability and reproducibility of our results.

Customization: We understand that every project is unique, which is why we offer customizable solutions tailored to your specific requirements. 

Speed: With our fast turnaround times and efficient workflows, we ensure the highest recovery without compromising quality, accelerating your research and development processes.

Cost-Effectiveness: We provide cost-effective solutions without compromising on quality, helping you maximize your budget. 

Neopharm answers to common questions about Chromatography

We specialize in a wide range of chromatographic methods, including HPLC, UPLC, SFC, GC, and more. Our expertise covers both achiral and chiral separations, catering to diverse analytical needs.

Our method development process is highly collaborative, tailored to the unique characteristics of each compound. We prioritize optimization for sensitivity, selectivity, and reproducibility, ensuring robust chromatographic methods that meet your analytical objectives.

At Neopharm, we employ a variety of analytical techniques, including HPLC, SFC, and preparative chromatography, to develop effective methods for chiral separation. Our team customizes each method based on the specific requirements of your compounds, ensuring optimal resolution and purity.

Our pharmaceutical impurity analysis services are backed by state-of-the-art instrumentation and rigorous quality control measures. We adhere to industry standards and regulatory guidelines, conducting thorough method validation and verification to ensure the accuracy, precision, and reliability of our results.

Absolutely. Our preparative chromatography capabilities extend to large-scale purification of enantiomers, allowing for the isolation and collection of target compounds in quantities suitable for further development and commercialization. Whether you require milligram to kilogram scale purification, we have the expertise and infrastructure to meet your needs.

Contact us today to learn more about our chromatography services and how we can support your analytical needs.

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