Method development and validation of pharmaceutical dosage forms is a core area of quality control to assure the desired specifications in terms of strength, quality, purity, and identity of dosage form. The quality and safety of drugs can be maintained by estimating and monitoring the impurities effectively to assure that safe and effective drug formulations are available to consumers. High Performance Liquid Chromatography is the most versatile tool for the qualitative and quantitative analysis of drugs for analysis.

Working as Assistant Professor in MMCP, Mullana. Passed B. Pharmacy from GGSCOP, Yamunanagar; M Pharmacy from GJUS&T, Hisar.Teaching experience of 5 yrs. More than 15 national/international publications and participated in many conferences.Won best podium presentation in ICPS-2014.Guided many research students.Member of various academic association