Sonali Patil

1)Preparation & submission of regulatory documents and ensuring compliance with Emerging & regulated markets. 2)Prepare & review the technical documents (AMV, PV, BMR, SPEC STP and CDP etc) and legal documents. 3)Ensure that all requirements meet the client & market requirements. Coordinating effectively with all cross functional teams to produce the documents required for compilation of dossiers. 4)Database & status maintaining. Keep all documents in respective folders & tracking updated. 2)As an apprentice in a drug metabolism, pharmacokinetics, and bioanalytical lab, my role is to support the work of the lab and learn as much as possible about drug development and analysis. I work closely with experienced scientists and technicians, and my work would be crucial to the success of ongoing research projects.