Two Months Pharamacovigilance Certification Course by Industry Professionals. Learn
• Clinical research process
• Planning a clinical trial
• Preparing essential documents: Protocol, CRF, IB, ICD
• EC & Regulatory submission
• Trial Management
• SAE Reporting
• Trial Monitoring
• Drug Safety Terminology
• Causality Assessment
• Guidelines for PV - ICH, WHO
• Regulations - the US, EU perspective
• Case Processing: Triage, Process, Report
• Working with MedWatch, CIOMS Forms, and literature sources
• Aggregate reporting
Join Extensive Training On Pharmacovigilance.
For More Details Visit: www.bcri.in/ph...
Негізгі бет Pharmacovigilance Course Overview at BCRI Bangalore
Пікірлер: 31