2-day In-person Seminar on Statistics for the Non-Statistician at Sao Paulo, Brazil
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Category Seminar, Health, Medical, Pharma, Clinical
Deadline: March 06, 2014 | Date: March 07, 2014-March 08, 2014
Venue/Country: Sao Paulo, Brazil, Brazil
Updated: 2014-01-27 15:45:38 (GMT+9)
Call For Papers - CFP
Overview: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 ? AgendaLecture 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 AnalysisExercise: 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 estimationLecture 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 ? AgendaExercise: Mock Experimental DesignLecture 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 frameworkExercise: Review and Critique a Sample SPC Control ChartLecture 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 powerExercise: Create a Mock Sampling PlanLecture 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 effectivelyWho 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 fieldsThe employees who will benefit include:? Development Scientists? Analytical Method Development? QA/ QC personnelAbout Speaker: Mr. Steven Walfish brings is the founder and President of Statistical Outsourcing Services. He brings nearly 20 years of industrial experience providing statistical solutions to complex business problems. Mr. Walfish was Senior Manager Biostatistics, Nonclinical at Human Genome Sciences in Rockville MD. Mr. Walfish has held positions with PricewaterhouseCoopers, Chiron Diagnostics and Johnson & Johnson. Mr. Walfish holds a Bachelors of Arts in Statistics from the University of Buffalo, Masters of Science in Statistics from Rutgers University and an Executive MBA from Boston University.DATE, VENUE & PRICE:Location : Zürich, Switzerland | 3rd & 4th March 2014| 9 AM to 6 PM Venue : Hilton Zurich Airport Address : Hohenbuehlstrasse 10, 8152 Opfikon Glattbrugg Zurich SwitzerlandPrice: $1,595.00Register now and save $200. (Early Bird)Until January 25, Early Bird Price: $1,595.00 From January 26 to March 01, Regular Price: $1,795.00 Location : Sao Paulo, Brazil | 6th & 7th March 2014| 9 AM to 6 PM Venue : WILL BE ANNOUNCED SOONPrice: $1,595.00Register now and save $200. (Early Bird)Until January 31, Early Bird Price: $1,595.00 From February 01 to March 04, Regular Price: $1,795.00Contact Information Event CoordinatorToll free: 1800 447 9407Fax: 302 288 6884Email: support
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Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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