Priyanka Pajai M.V.Sc ERT

Write and review various safety reports (or part of such reports) for global regulatory submissions, including but not limited to Annual Reports (IND and others), Periodic Safety Update Reports, Periodic 2. Adverse Drug Experience Reports, Periodic Benefit-Risk Evaluation Reports, Development Safety Update

Conduct toxicological risk assessments (TRAs) to support the biological evaluation of medical devices and develop responsesto submission deficiencies/questions. 2. Review literature and identify relevant articles to support product development and registration. writing of BEP and BER

. Toxicology Risk assessment for raw materials and formulations for cosmetics applications including Margin of Safety calculations and approval of products. 2. Literature search & safety data collection for identified chemicals 3. Literature review for hazard assessment of ingredients