High-quality Solutions for Purifying Pharmaceutical Compounds
At Neopharm, we understand the critical role of purification in the drug development process. Our Purification Solutions are meticulously designed to address the unique challenges faced by pharmaceutical researchers and manufacturers.
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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.
Contact usExperience and Expertise
With years of experience in the field, Neopharm has established itself as a trusted partner in purification solutions. We have successfully tackled a wide range of purification needs, leveraging our extensive knowledge and expertise in preparative High-Performance Liquid Chromatography (HPLC) and Supercritical Fluid Chromatography (SFC) systems. Our team of experts is adept at navigating the complexities of purification, delivering exceptional results with efficiency and reliability.
Our Services
Bulk Purification Services
We excel in purifying compounds at bulk scale, ensuring high purity and yield for your production needs.
Natural Products Purification
Our purification services are tailored for isolating natural products, offering high purity extracts for further analysis and development.
Purified Compound Libraries
We provide comprehensive library purification services to support your early-stage drug discovery projects. Our expertise lies in isolating and purifying compound libraries with the highest level of quality and purity, enabling you to streamline your screening efforts and identify promising lead compounds more efficiently.
Chiral Chromatography
With expertise in chiral separation, we offer purification services for resolving enantiomers and obtaining optically pure compounds.
Customized Chromatography Solutions
Our purification methods are customizable to your specific requirements, ensuring optimal purification efficiency and yield.
The Neopharm Solution
Expertise: Our team of chromatography experts specializes in compound purification and isolation techniques.
Reliability: We ensure the reliability and reproducibility of our purification methods, delivering high-quality purified compounds.
Customization: We offer tailored purification solutions to meet your unique compound purification needs.
Efficiency: With efficient purification workflows, we provide fast turnaround times and expedite your research and development processes.
Cost-Effectiveness: Our purification services offer cost-effective solutions without compromising on quality, helping you optimize your budget.
Collaborative Approach: We believe in fostering strong partnerships with our clients. Through open communication and collaboration, we work together to achieve your purification goals.
Neopharm answers to common questions about purification for pharmaceutical compounds
We have experience purifying a wide range of compounds, including small molecules, peptides, and oligonucleotides with multiple chiral centers.
We offer two key strategies to guarantee the highest level of purity:
1. Quality Control (QC) Assessment: We can simply transfer in and use your existing QC method or develop customized ones tailored to your specific needs. By employing a project applicable level of analytical rigor, we meticulously evaluate the purity of the purified compounds, ensuring accurate and precise results are being reported.
2. Cross-Contamination Prevention: We understand the potential risks associated with cross-contamination. To address this concern, we adhere to stringent protocols before starting a project, we implement thorough cleaning procedures for all systems and columns. This rigorous approach minimizes the risk of cross-contamination, safeguarding the integrity and purity of your compounds throughout the purification process.
Yes, our state-of-the-art facilities are equipped to handle purification projects of varying scales, from small-scale research to large-scale production.
The duration of the purification process depends on various factors, including the complexity of the compound and the scale of the project. We work closely with our clients to establish timelines that meet their needs and expectations.
We utilize a range of analytical techniques, including HPLC, GC, LC-MS, NMR, and more, to verify the purity of our purified compounds.
We have experience purifying a wide range of compounds, including small molecules, peptides, and oligonucleotides with multiple chiral centers.
We offer two key strategies to guarantee the highest level of purity:
1. Quality Control (QC) Assessment: We can simply transfer in and use your existing QC method or develop customized ones tailored to your specific needs. By employing a project applicable level of analytical rigor, we meticulously evaluate the purity of the purified compounds, ensuring accurate and precise results are being reported.
2. Cross-Contamination Prevention: We understand the potential risks associated with cross-contamination. To address this concern, we adhere to stringent protocols before starting a project, we implement thorough cleaning procedures for all systems and columns. This rigorous approach minimizes the risk of cross-contamination, safeguarding the integrity and purity of your compounds throughout the purification process.
Yes, our state-of-the-art facilities are equipped to handle purification projects of varying scales, from small-scale research to large-scale production.
The duration of the purification process depends on various factors, including the complexity of the compound and the scale of the project. We work closely with our clients to establish timelines that meet their needs and expectations.
We utilize a range of analytical techniques, including HPLC, GC, LC-MS, NMR, and more, to verify the purity of our purified compounds.
Contact us today to learn more about how our Purification Solutions can support your drug development initiatives.
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