Implementing Risk-based Verification for Pharmaceutical Manufacturing Companies 2013 is a webinar that covers topics such as:
- 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
Implementing Risk-based Verification for Pharmaceutical Manufacturing Companies 2013 brings together attendees from Pharmaceutical and life sciences industry involved in Project Management, Engineering, Quality Assurance, Commissioning and Qualification, Manufacturing and Operations and Regulatory Affairs.
