Combo of PV+CR+CDMS+Medical Writing

Service Description

This Training Program (3 Month Duration) will Include Module 1: Introduction to Pharmacology, Clinical Trials and Pharmacovigilance Module 2: Adverse Drug Reactions and Safety Reports Module 3: Methodologies in Pharmacovigilance Module 4: Management Systems and Drug Dictionaries in Pharmacovigilance (Argus, ArisG, MedWatch, MedRA, WHODD etc.) Module 5: Seriousness & Expectedness & Causality Assessment Criteria Module 6: Aggregate Safety Reports Module 7: Pharmacovigilance Regulations in Various Countries Module 8: Pharmacovigilance Programme in India (PVPI) Module 9: Signal Detection and Data Mining Module 10: Pharmacovigilance of Herbal Drugs & Medical Devices Module 11: Pharmacovigilance Compliance and Inspections Module 12: Hands-on training on Argus, ArisGlobal, ABcube etc software platforms. Module 13: Case Study Many Other Topic of Medical Writing, Clinical Research, and CDMS.