Strategies for Reducing Process Risk Increasing Yield, Reducing COGS and Improving Compliance
01:30 PM ET | 10:30 AM PT | 12:30 PM CT Duration 90 Minutes
Webinar Includes : All the training handouts , certificate ,Q/A and 90 mins Live Webinar
" Ron Snee is the Founder and President of Snee Associates, a firm dedicated to successful implementation of process and organizational improvement initiatives"
What does it mean to reduce risk, to manage risk, and how do you do it?
A critical source of risk to patients using pharmaceuticals to improve their health is inadequate design and control of the processes that manufactured the drugs. R&D, Manufacturing, Quality Assurance, Quality Control and Regulatory Affairs play a critical role in reducing risk associated with poorly operating processes. The ICH guidance documents Q8, Q9 and Q10 has heightened awareness in the pharmaceutical and biotech industries of the need to reduce process risk. This trend is also being promoted by the FDA as an approach to process improvement with the benefit of enhanced regulatory flexibility. But the questions remain: What does it mean to reduce risk, to manage risk, and how do you do it? Fortunately we have a lot of experience on which to draw.
Why Should you Attend
In this webinar our speaker Ron Snee will discuss the strategies and the associated guiding principles and illustrated with examples and case studies from the pharma and biotech industries. The focus is on reducing risk to reducing cost of goods sold (COGS) while improving process yield and compliance. The discussion also addresses how to make the use of process risk analysis and risk management an integral part of your process management systems, methods and tools.
• Utilizing the relationship between process variation, process understanding, process risk and compliance
• Using a systematic approach to identify the critical few variables that have a major impact on the process: Raw materials, process steps, and process variables and uncontrollable (environmental) variables
• Increasing process stability and capability
• Creating a process control strategy
• Robustness studies of the product and process
• Improvement of measurement performance including improved control and robustness of analytical methods
Who will Benefit
• Production managers
• Process Improvement Professionals
• Quality Engineers
• Quality Control and Lab Testing Personnel
• Research and Development Scientists
• Biologists and Microbiologists
• Chemists and Chemical Engineers
• Process and Manufacturing Engineers
• Quality Assurance Managers, Scientists and Engineers
• Regulatory Affairs Professionals
Industries who can attend
This 90-minute online course is intended for professionals in the Medical Device, Biotechnology,Pharmaceutical Industry. Although not presently stated in the draft , the same guide could be used by FDA Regulated Industries personnel