Prashant Avinash Patil
About Candidate
As a dedicated Research Associate at Nalanda Research Laboratories (USFDA Approved), I bring over 6 years of specialized experience in Analytical Development. My expertise lies in method development, method validation, and batch analysis of Nitrosamine and NDSRI impurities using advanced LCMS/MS techniques for drug substances and drug products. My role involves the meticulous identification and investigation of both known and unknown impurities, ensuring compliance with regulatory standards. I have undergone extensive training in 21CFR, equipping me with the knowledge to meet stringent quality requirements and contribute to the safety and efficacy of pharmaceutical products. Driven by a passion for precision and innovation, I am committed to advancing analytical methods that address the evolving challenges in impurity profiling. My work not only supports regulatory compliance but also enhances the overall quality of life by ensuring the purity of essential medications.
