Experienced in drug safety with focus on case processing, data entry, and medical coding. Strengths lie in understanding of pharmacovigilance protocols and regulatory guidelines, along with strong attention to detail and ability to manage multiple tasks. Proven track record in improving efficiency of reporting processes and maintaining high levels of data accuracy.
M. Pharm Research Project, Pharmacological evaluation of Bioactive compound in animal model of post-traumatic stress disorder, Searching databases such as PubMed, Cochrane Central Register of controlled Trial, Google scholar, medical council research register, shodhganga, National Research register, National clinical Trials, current controlled Trials, Conducting Meta-analysis by pooling data of effects of interventions from multiple studies for quantitative assessment.