Implementing Risk-based Verification for Pharmaceutical Manufacturing Companies 2013

Key Topics

• Industry standards and guidance documents addressing Science- and Risk-based verification (and project delivery overall)
• The reasons why risk-based verification processes are currently being adopted in industry
• Activities / phases in the System Lifecycle
• Differences between a traditional Commissioning and Qualification program and a risk based verification program
• Key considerations for implementation
• Activities, phases, and supporting practices in the science- and risk-based process as defined in ASTM E-2500

Who should Attend

Attendees from Pharmaceutical and life sciences industry involved in Project Management, Engineering, Quality Assurance, Commissioning and Qualification, Manufacturing and Operations and Regulatory Affairs.