Kavita Garg has over 12 years of experience working in a leading clinical research organizations (CROs) in all the phases of clinical studies. Additionally, she has 3.2 years’ experience in a leading Indian Pharma Company. She has experience in writing and editing clinical trial documents like protocols and amendments, clinical study reports (full and abbreviated), and scientific manuscripts for all phases of clinical trials. She also has experience in writing medico-marketing documents including presentations for scientific conferences and continuing medical education (CME) and performing quality control (QC) and review of regulatory documents as well as statistical analysis plans. Her main therapeutic area experiences include: cardiovascular disorders, central nervous system, diabetes mellitus, hematology, infectious diseases, oncology, pain management, and vaccines (influenza).

Clinical trial design, ICH-compliant clinical regulatory documents, safety reports, manuscript preparation