AGENDA
SPONSORS
Implement Patient-Focused Statistics Across the Process Validation Lifecycle
August 24, 2022
7:15 am PT – 4:15 pm PT
The Hilton Gaslamp I San Diego, CA or Online
FDA’s 3-Stage life cycle approach is the backbone of all validation and is globally recognized as the gold standard. Statistics and statistical methods are mentioned 14 times throughout FDA’s 19-page Process Validation Guidance. Although the concept was introduced in 2011, industry still struggles with using statistics effectively throughout the validation life cycle. KENX is proud to present this virtual training led by industry’s leading statisticians and Subject Matter Experts. Whether a statistics novice or a Six Sigma Black Belt, this seminar teaches statistics to validation and quality professionals how to master validation statistics throughout the process validation lifecycle.
Top Reasons to Attend
- Use Statistics as a Risk-Analysis Tool Throughout the PV Lifecycle
- Statistics in Process Development – Accelerate Development of a Robust Control Strategy
- Determine Proven Acceptable Ranges (PARs) or Design Space
- Use of Modern Statistical Tools for Accelerated Development & Novel Therapies
- Link Knowledge Across the Lifecycle & Optimize in PPQ
- Develop Sampling Plans to Demonstrate Process Performance
- Define Statistical Confidence and Relate to Sample Size and Statistical Uncertainty
- Design PPQ Sampling Plans for Continuous and Pass/fail Attributes
- Describe a Risk-based Approach to Determining the Number of PPQ Batche
- Develop a Control Strategy Using Design of Experiments (DOE)
- Learn Key Elements in Designing a Continued/Ongoing Process Verification Program
- Develop a Targeted, Practical Approach to Enhanced Sampling During
- Understand Key Components of Commonly Used Control Charts
- Overcome leptokurtophobia (irrational fear of non-Normality)
- Learn to Be a Statistical Sleuth with Exploratory Data Analysis & Statistical Thinking
- Learn How to Avoid Pitfalls When Using Historical Data
Personnel in the Following Environments Should Attend:
- Process Validation
- QA/QC
- Engineering
- Process
- Design Control
- Product Development
- Regulatory Affairs
- Process Scientist
- Six Sigma Green Belt and Black Belt
- Continuous Improvement Manager
- Statistician
- Regulatory Affairs
- Manufacturing
- Laboratory
This event is also appropriate to business development and sales managers that offer innovative solutions for quality validation and engineering professionals in the life science industry.