Precise Isolation, Exceptional Results

During drug development, addressing impurity challenges is crucial. Our Targeted Isolation™ method streamlines and minimizes costs for efficient drug development.

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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 commitment is to collaborate closely with our clients, understanding their unique needs and concerns in pharmaceutical research, drug discovery, and quality control.

We meticulously select the most suitable methods tailored to your specific projects. Our specialized knowledge and capabilities ensure accurate and reliable results, whether isolating trace impurities or profiling complex mixtures.

Our Services

Impurities Isolation:

- Trace Component Isolation

Delve deep into your drug substances with our cutting-edge technology, extracting impurities as low as 0.01% of bulk, guaranteeing unparalleled purity and safety.

 - Multiple Impurities from a Single Lot

Maximize efficiency and resource consumption by isolating multiple impurities from a single source, streamlining your purification process without compromising on quality.

  - Enriched Impurity Extracts

Gain invaluable insights into impurity profiles with our enriched impurity extracts, providing a comprehensive foundation for thorough analysis and characterization, empowering informed decision-making.

 - Unique, Scalable Strategy 

Benefit from our tailored approach, meticulously designed to adapt seamlessly to your project's evolving needs, ensuring scalability without sacrificing precision or reliability.

- Batch Scale Chromatography

Harness the power of advanced chromatographic techniques to achieve consistent and reproducible results, utilizing batch scale chromatography to unlock new possibilities in impurity isolation and purification.

Impurities Profiling:

- Full Structure Elucidation 

Understand your drug substances with our comprehensive approach, utilizing state-of-the-art 2D NMR and accurate mass MS/MS techniques to reveal the full structural composition of isolated impurities, providing clarity and confidence.

 - Verification of Identity

Rest assured in the accuracy and reliability of our services, as we meticulously verify the identity of isolated impurities through rigorous validation processes, ensuring the integrity and authenticity of your results.

 - Stress Degradation Studies: 

Stay ahead of potential risks and challenges with our thorough stress degradation studies, meticulously assessing impurity behavior under various stress conditions to guarantee stability and safety throughout the drug development process.

 - Physical Property Testing: 

Gain a deeper understanding of impurity characteristics and behavior with our comprehensive physical property testing, allowing for precise evaluation and analysis to inform critical decisions and optimizations.

The Neopharm Solution

At Neopharm, we recognize the critical importance of accurate impurity isolation and profiling in the pharmaceutical industry. Our comprehensive approach is designed to address the unique challenges faced by drug developers, ensuring the highest standards of purity and safety throughout the development process.

Tailored Precision: We employ advanced techniques tailored to the specific needs of each project, ensuring precision in isolating and characterizing impurities with unparalleled accuracy.

In-depth Profiling: Our expert team utilizes cutting-edge methodologies, including 2D NMR and accurate mass MS/MS, to provide comprehensive profiling, enabling a deep understanding of impurity structures and behavior.

Rigorous Verification: Every isolated impurity undergoes rigorous verification processes to confirm its identity, ensuring reliability and consistency in our results.

Stability Assurance: Through stress degradation studies, we evaluate impurity behavior under various conditions, providing crucial insights into stability and safety considerations.

Efficiency and Scalability: Our streamlined processes and scalable strategies optimize resources, delivering efficient results without compromising quality or timelines.

With Neopharm's Impurity Isolation & Profiling Services, you can trust in our commitment to excellence, precision, and reliability at every stage of your drug development journey.

Neopharm answers to common questions about Impurity Isolation & Profiling Services

Our Targeted Isolation™ methodology is designed to meet the unique challenges of pharmaceutical development. By isolating unknown chemical impurities with unparalleled precision and efficiency, we help streamline development processes, reduce costs, and accelerate time-to-market for drug substances and products.

At Neopharm, we set ourselves apart with our innovative approach to impurity isolation and profiling. Our use of advanced techniques such as 2D NMR, accurate mass MS/MS, and stress degradation studies ensures thorough characterization and verification of impurities, providing valuable insights for drug development.

Our unique, scalable strategy in batch-scale chromatography allows us to adapt to varying project requirements while maintaining reliability and reproducibility. Whether isolating trace components or multiple impurities from a single lot, our chromatography services deliver consistent results, ensuring the integrity and purity of pharmaceutical products.

Contact us today to learn more about our Impurity Isolation & Profiling Services and how we can support your analytical needs.

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