 The competent Pharmacovigilance professional with 10 years of experience in clinical safety comprising of 7 years of experience in Pharmacovigilance/Drug Safety and three years in clinical practice & individual patient management
 7 years of hardcore experience in end to end Pharmacovigilance vis-à -vis team management, subject matter expertise & quality assurance activities pertaining to pharmaceutical medicines (drugs), monograph products, devices; managing Adverse Event reports& Device malfunctions
Specialties:
Pharmacovigilance/Drug Safety:
End to end Case Processing
Aggregate Safety Report writing
Operational Management
Quality Management,