RAPS Approved Seminar on Risk Management in Pharmaceutical Industry 2012

Risk Management in Pharmaceutical Industry is a seminar dedicated to methods, processes and tools associated with Quality Risk Management (QRM), including topics such as:

• Introduction to QRM
• QRM`s broader context
• Risk Assessment Overview
• Systems Approach to QRM
• Risk Control
• Risk Identification
• Selection & use of QRM Tools
• Risk Communication
• How is QRM audited and how to defend a QRM Audit
• Integrating QRM into QMS

Who should Attend

Quality Compliance Professionals, Middle and upper level managers, Production Managers, R&D and Technology Transfer Personnel, Engineering and IT, Manufacturing, Validation Service Providers, R&D Personnel, Pharmaceutical/Medical Device/Healthcare /Engineering personnel and Clinical Development.