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.
