Accelerate your Research and Development Efforts
Neopharm offers advanced analytical techniques to help you identify unknown contaminants and characterize common impurities.
Contact Us
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 usAt Neopharm, we provide thorough Impurities Identification services that accurately analyze and identify impurities in pharmaceutical products. Our team of experts uses advanced techniques and instruments to determine the nature and source of impurities, helping you meet regulatory standards, maintain product safety, and uphold quality standards. You can trust Neopharm to offer meticulous impurities identification to safeguard patient health and maintain your brand reputation.
THE NEOPHARM SOLUTION
Identify Structure with Accuracy & Efficiency
We use UPLC-MS/MS technology to confirm the structure of impurities, allowing you to conduct pharmacologic or toxicologic studies with greater accuracy and efficiency. We will also provide you with a report on the levels of impurities in the sample. This allows you to identify any potential sources of contamination which can lead to potential product recalls.
Comprehensive Analysis
We offer a wide range of services to help you characterize possible impurities in your products.
UPLC coupled with diode assay and CAD detection, for characterization of chromophore and response factor. This technique gives us the ability to identify and quantify compounds with high sensitivity and specificity, allowing us to provide useful information for various applications.
We have expertise in Gas Chromatography/Mass Spectrometry (GC/MS) and Flame Ionization Detection (FID) for the analysis of volatile impurities in pharmaceuticals, and other samples. Our advanced equipment and knowledgeable scientists allow us to deliver precise results in a timely manner. We take great pride in our dedication to delivering high-quality services and providing complete customer satisfaction.
We provide accurate and reliable results to detect metal impurities through Inductively Coupled Plasma Mass Spectrometry (ICP-MS). This tool can detect even minimal amounts of trace metals. Hence, it is ideal for numerous applications like environmental monitoring, determining the quality and safety of products, pharmaceutical analysis, and food safety testing.
Rapid Characterization
We offer rapid impurity characterization to help identify potential contaminants and make informed decisions about drug safety. Our analysis provides valuable insights into impurities and enhances quality control measures for safe and reliable pharmaceutical products.
Accelerate Your Research and Development Efforts
Our expert analysis provides you with critical information on the nature and source of impurities present in your formulations. By proactively addressing impurity concerns during the development stage, you can optimize formulation strategies, meet regulatory requirements, and ensure the safety and efficacy of your future products.
Additionally, our laboratory experts are daily working on:
- Ions visual identification tests
- Infrared and Ultraviolet identification
- Appearance, solubility, colour, and turbidity tests
- Chemical identification
- USP General identification tests
- EP identification tests; and more.
Neopharm Answers to Common Questions About Impurities Identification
Impurities can arise from various sources such as raw materials, synthesis processes, or degradation of the drug substance or product. Identifying and characterizing impurities is crucial to ensure product safety, efficacy, and regulatory compliance. It allows for risk assessment, understanding the impact on product quality, and implementation of appropriate control measures.
Neopharm employs a range of advanced analytical techniques, including chromatography (HPLC, GC), mass spectrometry (MS), nuclear magnetic resonance (NMR), and spectroscopy, among others. These techniques enable us to separate, identify, and characterize impurities present in pharmaceutical products accurately. Our experienced team follows validated methods and stringent quality control measures to ensure precise and reliable results.
Absolutely. Neopharm has extensive experience in handling impurities identification for a wide range of pharmaceutical formulations, including complex and challenging matrices. Whether you require analysis for small molecules, biologics, or combination products, our team has the expertise and resources to handle the complexity and provide accurate characterization of impurities.
The timeframe for impurities identification testing can vary based on factors such as the complexity of the sample, the number of impurities, and specific testing requirements. At Neopharm, we understand the importance of timely results. During our initial consultations, we will discuss project timelines and provide you with realistic estimates to ensure effective planning and alignment with your objectives.
Impurities can arise from various sources such as raw materials, synthesis processes, or degradation of the drug substance or product. Identifying and characterizing impurities is crucial to ensure product safety, efficacy, and regulatory compliance. It allows for risk assessment, understanding the impact on product quality, and implementation of appropriate control measures.
Neopharm employs a range of advanced analytical techniques, including chromatography (HPLC, GC), mass spectrometry (MS), nuclear magnetic resonance (NMR), and spectroscopy, among others. These techniques enable us to separate, identify, and characterize impurities present in pharmaceutical products accurately. Our experienced team follows validated methods and stringent quality control measures to ensure precise and reliable results.
Absolutely. Neopharm has extensive experience in handling impurities identification for a wide range of pharmaceutical formulations, including complex and challenging matrices. Whether you require analysis for small molecules, biologics, or combination products, our team has the expertise and resources to handle the complexity and provide accurate characterization of impurities.
The timeframe for impurities identification testing can vary based on factors such as the complexity of the sample, the number of impurities, and specific testing requirements. At Neopharm, we understand the importance of timely results. During our initial consultations, we will discuss project timelines and provide you with realistic estimates to ensure effective planning and alignment with your objectives.
Choose Neopharm for precise and comprehensive Impurities Identification services that prioritize patient safety, regulatory compliance, and product quality. Contact us today to ensure the purity of your pharmaceutical products.
Contact us