Description:
In Guidance for Industry Process Validation: General Principle and Practices, process validation is defined as, ""...the collection and evaluation of data, from the process design stage through commercial production." The guidance further delineates the 'process design stage through commercial production' into three distinct stages of the product lifecycle:
Stage 1: Process Design: The commercial manufacturing process is defined during this stage based on knowledge gained through development and scale-up activities.
Stage 2: Process Qualification: During this stage, the process design is evaluated to determine if the process is capable of reproducible commercial manufacturing.
Stage 3: Continued Process Verification: Ongoing assurance is gained during routine production that the process remains in a state of control.
The first stage of process validation is process design. The Process Validation guidance document states, "A successful validation program depends on information and knowledge from product and process development. This knowledge and understanding is the basis for establishing an approach to control of a manufacturing process that results in products with desired quality attributes:
Manufactures should:
Understand the sources of variation
Detect the presence and degree of variation
Understand the impact of variation on the process and ultimately on product attributes
Control the variation in a manner commensurate with the risk it represents to the process and product."
The second stage of process validation is process qualification. Although stage 2 has two elements, this course will focus on recommendations for the second element, PPQ. PPQ "combines the actual facility, utilities, equipment (each now qualified), and the trained personnel with the commercial manufacturing process, control procedures, and components to produce commercial batches." Additionally, the process validation guidance document that "Each manufacturer should judge whether it has gained sufficient understanding to provide a high degree of assurance in its manufacturing process to justify commercial distribution of the product. Focusing exclusively on qualification efforts without understanding the manufacturing process and associated variations may not lead to adequate assurance of quality."
The third stage of process validation is continued process verification. The process validation guidance document defines the need for this stage: "After establishing and confirming the process, manufacturers must maintain the process in a state of control over the life of the process, even as materials, equipment, production environment, personnel, and manufacturing procedures change." Manufacturers should use ongoing programs to collect and analyze product and process data to evaluate the state of control of the process. These programs may identify process or product problems or opportunities for process improvements that can be evaluated and implemented through some of the activities described in Stages 1 and 2."
This course focuses on how to establish a systematic approach to implementing statistical methodologies into a process validation program consistent with the FDA guidance. It begins with a primer on statistics, focusing on methods that will be applied in each remaining chapter. Next, it teaches the application of statistics for setting specifications and assessing measurement systems (assays), two foundational requirements for process validation. Lastly, the course applies statistic through the three stages of process validation defined by requirements in the process validation regulatory guidance documents. Methods taught through all three stages are recommended by regulatory guidance documents; references to the specific citations in the guidance documents are provided.
Why you should attend:
The Food and Drug Administration (FDA) provided a guidance for industry in 2011 that has established a framework for process validation in the pharmaceutical industry. This guidance, titled "Process Validation: General Principles and Practices" consists of a three-stage process. The three stages are 1) Process Design, 2) Process Qualification, and 3) Continued Process Verification.
This course focuses on how to establish a systematic approach to implementing statistical methodologies into a process development and validation program consistent with the FDA guidance. This course teaches the application of statistics for setting specifications, assessing measurement systems (assays), using design of experiments (DOE), developing a control plan as part of a risk management strategy, and ensuring process control/capability. All concepts are taught within the three-stage product cycle framework defined by requirements in the process validation regulatory guidance documents.
Although established for the pharmaceutical industry, it also provides a useful framework for other industries.
Analyses in this course use the point-and-click interface of JMP software by SAS.
Areas Covered in the Session:
Apply statistics to set specifications and validate measurement systems (assays)
develop appropriate sample plans based on confidence and power
implement suitable statistical methods into a process validation program for each of the three stages
Stage 1, Process Design: utilize risk management tools to identify and prioritize potential critical process parameters; and define critical process parameters and operating spaces for the commercial manufacturing process using design of experiments (DOE)
Stage 2, Process Qualification: assess scale effects while incorporating large (pilot and/or commercial) scale data; develop process performance qualification (PPQ) acceptance criteria by characterizing intra and inter-batch variability using process design data and batch homogeneity studies; and develop an appropriate sampling plan for PPQ
Stage 3, Continued Process Verification: develop a control plan as part of a risk management strategy; collect and analyze product and process data; and ensure your process is in (statistical) control and capable.
Who Will Benefit:
This seminar is designed for pharmaceutical and biopharmaceutical professionals who are involved with product and/or process design, validation, or manufacturing/control.
Process Scientist/Engineer
Design Engineer
Product Development Engineer
Regulatory/Compliance Professional
Design Controls Engineer
Six Sigma Green Belt
Six Sigma Black Belt
Continuous Improvement Manager
Agenda:
Day 1 Schedule
Lecture 1:
Introduction to Statistics for Process Validation
principles of process validation
stages of process validation
Primer on Statistical Analysis
basic statistics
Lecture 2:
Primer on Statistical Analysis (cont.)
statistical intervals and hypothesis testing
Lecture 3:
Primer on Statistical Analysis (cont.)
statistical intervals and hypothesis testing
ANOVA
Lecture 4:
Primer on Statistical Analysis (cont.)
regression
run charts
Day 2 Schedule
Lecture 1:
Foundational Requirements for Process Validation
setting specifications
analytical methodology
Stage 1 - Process Design
steps to DOE
screening designs
Lecture 2:
Stage 1 - Process Design
response surface designs
establishing a strategy for process qualification
Lecture 3:
Stage 2 - Process Qualification
introduction
incorporation of large-scale data
development of PPQ acceptance criteria
development of sampling plans
Lecture 4:
Stage 3 - Continued Process Verification
statistical process control
process capability
Speaker:
Richard (Rick) K. Burdick
Emeritus Professor of Statistics, Elion Labs
Richard (Rick) K. Burdick is an Emeritus Professor of Statistics, Arizona State University (ASU), where he instructed undergraduate and graduate students for 29 years. Following his tenure at ASU, Dr. Burdick was a Quality Engineering Director for Amgen Inc. for 10 years.
Dr. Burdick's research and consulting interests consider several CMC statistical applications including comparability studies, stability data analysis, analytical method validation, quality by design process characterization, and analytical similarity for biosimilar products. He has written over 60 journal articles and three books, including Confidence Intervals for Random and Mixed ANOVA Models with Applications to Gauge R&R Studies, (with C. M. Borror and D. C. Montgomery) and Confidence Intervals on Variance Components, (with F. A. Graybill).
Dr. Burdick is a Fellow of the American Statistical Association and a member of the American Society for Quality. He has served on the USP Statistics Expert Committee since 2010.
He received his bachelor’s Degree in Statistics from the University of Wyoming. He received his master’s and Doctorate degrees in Statistics from Texas A&M University.
Location: Philadelphia, PA Date: January 15th and 16th 2019 and Time: 9:00 AM to 6:00 PM
Venue: DoubleTree by Hilton Philadelphia Airport 4509 Island Avenue, Philadelphia, PA 19153
Price:
1 ATTENDEE $2,000 Regular Price: $2000 Register for 1 attendee
5 ATTENDEES $10,000 Regular Price: $10,000 Register for 5 attendees
10 ATTENDEES $20,000 Regular Price: $20,000 Register for 10 attendees
Until December 13, Early Bird Price: $2,000.
From December 14 to January 13, Regular Price: $2,200.
Use this promo code GCP50 to get 50% off.
Sponsorship Program benefits for seminar
For More Information- https://www.globalcompliancepanel.com/control/sponsorship
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