Understanding Compound Behavior for Enhanced Pharmaceutical Stability

Neopharm force degradation solution helps you understand how compounds degrade under various conditions, providing vital insights for product development, regulatory compliance, and overall safety. allowing you to make the most out of your pharmaceutical stability tests.

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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 specialize in forced degradation analytical methods and degradation pathway GMP services to ensure the safety and efficacy of your pharmaceutical products. 
Our analyses are specifically designed to identify impurities, degradation products, and other contaminants that may impact the quality of a product. We provide a complete set of analytical services to determine degradation pathways, analyze the characteristics of degradation products, and evaluate the stability of active ingredients in pharmaceuticals. We offer a variety of GMP-compliant services to aid in product stability investigations.


Efficient Insights

Our advanced forced degradation techniques let you assess the degradation pathways and chemical mechanisms of your compounds with ease — giving you an insight into their stability and helping you get to market faster.

Understand Your Compounds Better

Neopharm's analyses allow us to identify potential degradation pathways and determine the rate of degradation in various conditions — so that you can make informed decisions on your products' stability.

Accelerated Testing

Our methods accelerate the testing process, allowing you to anticipate potential stability issues and address them proactively.

Neopharm Answers to Common Questions About Stress Testing (Forced Degradation)

Forced degradation testing involves subjecting pharmaceutical compounds to harsh conditions like temperature, humidity, light, and chemical stressors to accelerate their degradation. This helps identify potential degradation pathways and degradation products.

Understanding degradation pathways provides crucial insights into the stability of pharmaceutical products. It helps in predicting potential degradation products, enabling you to design effective formulation strategies and extend product shelf life.

Neopharm specializes in forced degradation analytical methods and degradation pathway GMP services. Our expertise, advanced technology, and commitment to quality ensure accurate results for informed decision-making in the pharmaceutical industry.

Contact us today to learn more about our comprehensive suite of analytical services and how we can tailor them to your specific needs. Our team is dedicated to helping you achieve your goals efficiently and effectively.

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