Drug Safety Associate
Since October 2014
September 2013 --- September 2014
Ensuring all processes contributing to the performance of a clinical trial according to ICH-GCP guidelines. Manage and maintain databases for the quality system. Compile and prepare materials for submission to regulatory agencies. Document internal regulatory processes. Ensure regulatory rules are communicated through corporate policies and procedures.
January 2013 --- January 2014
M pharma in Advanced Pharmacology and Toxicology from Rajiv Gandhi University of Health Sciences in 2013
Bachelor's in pharmacy in Pharmaceutical Sciences from M.S. Ramaiha college of pharmacy in 2009