The Life Sciences Risk Management A to Z - Best Practices for Effectiveness and Efficiency: 2-Day Workshop 2016 covers topics such as:
- Regulatory requirements for application of risk principles
- General principles and approach to risk management
- How compliance and risk management are strategically used
- Key steps and activities for a risk management program
- How to classify cGMP non-conformances according to risk priority
- Principles and requirements of ICH Q9
- How to apply risk management principles in process design
- Hazard Analysis and Critical Control Point (HACCP) in production and process control
- The different tools applicable to risk management
- How to use HACCP tables to maintain process control of production lines
- How to apply risk management to validation
- Failure Mode and Effect Analysis (FMEA) for an example pharmaceutical product
The Life Sciences Risk Management A to Z - Best Practices for Effectiveness and Efficiency: 2-Day Workshop 2016 brings together attendees from the pharmaceutical and medical device industry involved in:
- Production
- Quality
- Validation
- R&D
- Risk
- Engineering
- Manufacturing
- Operations
- Project
