Designing and reviewing of Protocols Investigator Brochures Clinical Study Reports Manuscripts IMPDs Posters Medical Web Content REGULATORY AFFAIRS Submission of study protocol to Indian DCGI Assistance for Importing and Export trial product to India Dossiers Drug Master File (DMF) Electronic Common Technical Document (eCTD) Expert solutions to FDA queries Contract Management Quality Assurance BIOSTATISTICS Sample Size Calculation Randomization Clinical Trial Design