FDA Based Guidelines on Statistical Sampling Plans | August 7, 2014 8:30 AM - August 8, 2014 4:30 PM | Automation.com

FDA Based Guidelines on Statistical Sampling Plans

Event Summary

August 7, 2014 - August 8, 2014
Singapore, CA 238867
August 7, 2014 8:30 AM
August 8, 2014 4:30 PM
[email protected]
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This Seminar is Pre- approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.


Statistical tools and techniques are very commonly used to help measure and improve the quality of a firm's process and product. If statistical analysis is not properly performed and/or understood, a firm can run the risk of distributing the kind of product to the market that ultimately fails, resulting in lost time and money. And of course, with statistics, practice makes perfect. During this two-day HIGHLY interactive training program, participants will be given the opportunity to apply statistics learned to real-world example data sets! The program begins by providing a basic overview of the most common statistical tools and terms. The course covers the use of statistical software packages and the role of software in statistical analysis and statistical process control. Areas addressed include how to use statistics to properly trend data, support the annual product review, justify process changes and set product specifications. By the end of day two, course participants will have acquired the skills necessary to design a statistically sound sampling plan that helps them comply with FDA APR requirements.

Throughout the duration of this intimate, hands-on course, participants will be able to interact with both an expert instructor and their peers.

Why you should attend:

This course will help you to use statistics correctly and minimize compliance risk.

Course Description:

Day 1 – Agenda

Lecture 1: Introduction and Basic Overview of Common Statistical Tools
Exercise: Identify Participants' Statistical Experience and Course Goals
• Types of Data
• Data Presentation and Graphics
• Normal Distribution
• Introduction to Hypothesis Testing
• Discuss applicable software packages for use:

Lecture 2: Apply Statistics to Specification Setting
• Setting appropriate product specifications
• Determine FDA requirements for OOS results
• Determine how to best investigate OOS results
• Introduction to Interval Estimation
• Outlier Analysis
Exercise: Setting Statistical Based Specifications

Lecture 3: Regression analysis and variance components
• Correlation
• Linear models
• New Patient Rights
• Residual analysis
• Lack of fit
• Hazards of regression
• Multiple regression
• Non-linear regression (4-parameter models)
• Analysis of stability data including shelf life estimation
Lecture 4: Implement Design of Experiments (DOE)
• Design experiments appropriately and effectively
• Ensure that experiments are reproducible
• Improve process capability by reducing variability
• Analysis of variance

Day 2 – Agenda

Exercise: Mock Experimental Design
Lecture 5: Validate your Testing Methods using Statistics
• Analyze ICH guidelines (Q2A & Q2B)
• Ensure robustness and ruggedness of your method
• Develop protocols based on sound statistical methods
• Quantify validation characteristics:
• Regression analysis and variance components
• Analysis of Stability data.
Exercise: Analysis of a Method Validation Study Including Protocol Development
Lecture 6: Trending Analysis
• Define Statistical Process Control (SPC)
• Determine how SPC can be applied to and help your process
• Identify the benefits of using SPC
• Trend Analysis
• Comply with FDA Requirements for Process Analytical Technology (PAT)
• Define Process analytical technologies and identify related tools
• Identify the role statistics play in the PAT framework
Exercise: Review and Critique a Sample SPC Control Chart
Lecture 7: Design a Statistically Sound Sampling Plan
• Define different types of sampling
• Create and justify your sampling plan
• Account for sampling and measurement error
• Determine the relationship between sample size, statistical precision, and statistical power
Exercise: Create a Mock Sampling Plan
Lecture 8: Statistically Analyze Annual Product Review (APR) Data
• Examine statistical techniques relevant to APRs
• Use descriptive statistics to present the data
• Use graphs and plots effectively

Who Will Benefit:

This course is developed to provide valuable assistance to all regulated companies that need to understand their processes including companies:
• Medical Device
• Diagnostic
• Supervisors
• Pharmaceutical
• Biologics fields
The employees who will benefit include:
• Development Scientists
• Analytical Method Development
• QA/ QC personnel

About Speaker:

Steven Walfish
President, Statistical Outsourcing Services
Mr. Steven Walfish is the President of Statistical Outsourcing Services, a consulting company that provides statistical analysis and training to FDA regulated industries. Prior to starting Statistical Outsourcing Services, Mr. Walfish was the Senior Manager Biostatistics, Non-clinical at Human Genome Sciences in Rockville MD. Prior to joining HGS, Mr. Walfish was a Senior Associate at PricewaterhouseCoopers specializing in the pharmaceutical industry. Mr. Walfish was Manager of Non-Clinical Statistics at Chiron Diagnostics. Mr. Walfish brings over 20 years of industrial expertise in the development and application of statistical methods for solving complex business issues including data collection, analysis and reporting.


Location: Singapore Date: August 7th & 8th, 2014 Time: 8:30 AM to 4:30 PM
Venue Name: Mandarin Orchard Singapore 333 Orchard Road, Singapore 238867
Venue Address: Mandarin Orchard Singapore 333 Orchard Road, Singapore 238867

Price: $1,595.00

Register now and save $200. (Early Bird)
Until July 10, Early Bird Price: $1,595.00
from July 11 to August 05, Regular Price: $1,795.00

Contact Information

Event Coordinator
Toll free: +65 3158-1047
Fax: 302 288 6884
Email: [email protected]
Website: https://www.globalcompliancepanel.com
Event Link - http://bit.ly/StatisticsfortheNon-Statistician
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