Ensuring Safety and Quality in Pharmaceutical Products

Neopharm provides precise, reliable, and cost-effective impurity profiling and characterization services that help Chemistry, Manufacturing and Controls (CMC) teams make informed decisions to ensure the safety and efficacy of their products.

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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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At Neopharm, we prioritize understanding and addressing the specific needs of our customers. We recognize that risk assessments play a crucial role in ensuring the safety and efficacy of pharmaceutical products. With our customer-centric approach, we collaborate closely with you to provide tailored solutions that meet your unique requirements. Our team of experts brings together technical proficiency, regulatory knowledge, and a commitment to excellence to deliver comprehensive risk assessments that inspire confidence and drive success.


Accuracy & Reliability You Can Trust

We take pride in our expert team and advanced technology that enables us to provide accurate, reliable data on the quality, safety, and efficacy of our client’s products. Our comprehensive support covers all stages from preclinical to commercial development.

Faster & Better Product Launches

We understand how important it is for product development teams to get their products to market quickly and efficiently. With our comprehensive impurity profiling & characterization services, we can ensure faster turnaround times and better launches for your products.

Regulatory Compliance Made Easy

We provide consultancy services to help you with regulatory compliance, so you can be sure that your products meet all the required standards before they launch. We also provide training and guidance on industry best practices to maximize your success rate.

Discover our range of specialized risk assessment services tailored to meet your unique needs.

Nitrosamines Impurities Testing

Stay ahead of the evolving regulatory landscape by partnering with Neopharm for Nitrosamine Testing. Our state-of-the-art analytical methods and advanced instrumentation enable us to detect and quantify nitrosamine impurities in any type of pharmaceutical products. We employ robust methodologies, ensuring accurate and reliable results. Trust Neopharm to help you mitigate risks associated with nitrosamine impurities and maintain compliance with regulatory guidelines. Learn more

Extractables and Leachables Testing

Ensure the safety and compatibility of your pharmaceutical packaging and manufacturing processes with Extractables and Leachables Studies from Neopharm. Our comprehensive approach includes the identification, quantification, and toxicological assessment of potential extractables and leachables. By evaluating these substances, we help you mitigate the risks of contamination and ensure the integrity of your products. Learn more

Elemental Impurities

Rely on Neopharm for Elemental Impurities testing services to comply with rigorous regulatory requirements. We employ advanced analytical techniques to accurately determine the presence and concentration of elemental impurities in your pharmaceutical products. Our expertise in risk assessment and compliance enables you to navigate the complex landscape of elemental impurities with confidence and peace of mind. Learn more

Impurities Identification

Neopharm offers Impurity Identification services to help you detect and characterize unknown and unexpected impurities in your pharmaceutical products. Our state-of-the-art instrumentation and experienced scientists meticulously analyze your samples, providing valuable insights into impurity profiles and potential risks. Trust Neopharm to guide you through the identification and management of impurities, ensuring the safety and efficacy of your products. Learn more

Related Substances and Foreign Impurities

Neopharm provides comprehensive analysis and assessment of related substances and foreign impurities in pharmaceutical products. Our advanced analytical techniques enable us to identify and quantify impurities, ensuring compliance with regulatory guidelines and product quality standards. Partner with us to enhance your understanding of related substances and impurities, mitigating risks and maximizing the safety of your products. Learn more

PFAS Testing

Detecting per- and polyfluoroalkyl substances (PFAS) may not be a commonly discussed issue in the pharmaceutical field, but its potential impact on safety and compliance cannot be ignored. At Neopharm, we specialize in PFAS detection, offering comprehensive screening procedures designed specifically for the pharmaceutical industry, mainly for verification of your water system. Trust Neopharm to address this emerging concern and safeguard the integrity of your pharmaceutical products. Learn more

Impurity Isolation & Profiling Services

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

Purification Solutions for Pharmaceutical Compounds

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. Learn more

Improve your risk assessment capabilities and ensure the safety and quality of your pharmaceutical products. Partner with Neopharm today and leverage our expertise, advanced methodologies, and commitment to excellence. Contact us now to discuss your specific needs and discover how our specialized services can empower your pharmaceutical operations. 

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