RAPS Approved Seminar on Risk Management in Medical Devices Industry at Mumbai 2012

Topics

• Risk Management Life Cycle
• Risk Management Planning
• Hazard Domains
• Hazard Identification
• Risk Rating Methods
• Hazard Latency Issues
• Mitigation strategies and priorities
• Initial (unmitigated) Risk Assessment
• Alarm systems as mitigations
• Mitigation architectures
• Post mitigation risk
• Risk control bundles
• Safety Integrity levels
• Residual risk

RAPS Approved Seminar on Risk Management in Medical Devices Industry at Mumbai 2012 is designed to representatives from: Regulatory Affairs, Pharmacoepidemiology, Pharmacovigilance Specialists, Clinical Safety Staff, Quality Management Specialists, Regulatory Affairs Professionals, Regulatory Affairs, Drug Safety and Pharmacovigilance, Executives (including C-Level) with any legal responsibility for drug safety and Clinical Development.