At Alentris Research Private Limited, we are dedicated to advancing the field of impurity science since our founding in 2019. Our experienced team provides solutions for pharmaceutical, biopharmaceutical, and chemical companies seeking expertise in API Impurities, Working Standards, Analytical Standards, Degradation Impurities, Genotoxic Impurities, Organic Impurities, and satisfying Regulatory Requirements for impurity testing and identification.

Leveraging state-of-the-art analytical instrumentation and methodologies, we specialize in the Isolation and Characterization of both known and Unknown Impurities, enabling the Discovery of Impurities to support development, improve quality, and ensure safety.

With expertise in Impurity Research, our scientific team specializes in the custom Synthesis of Impurity standards including Nitrosamines Impurities, Oncology Impurities, and Peptide Impurities. We are dedicated to supporting pharmaceutical companies through expert Impurity services for drug development, quality control, and regulatory compliance.

We offer Force Degradation studies to assess impurity profiles and meet EP and USP Impurities guidelines. Our capabilities include Photolytic Degradation Impurity, Thermal Degradation Impurity, Oxidative Degradation Impurity, and Acid-Alkaline Degradation Impurity testing. For pharmaceutical companies, we provide impurity analysis and identification in drug substances, Formulation Impurities, degradation products, and more. Contact us to learn about our impurity management services for API and drug development.