Statistical Methods 2017 - Statistical Methods A Visual Approach 2017

Course "Statistical Methods: A Visual Approach" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.
Overview:
An essential task in any compliance analytics workflow is to not only explore your data visually, but also to communicate your results professionally with graphic displays. Do you have the tools and skills to quickly and thoroughly perform these tasks? This course in data visualization will present methods to allow you to interactively discover relationships graphically. We will provide the foundations for creating better graphical information to accelerate the insight discovery process and enhance the understandability of reported results. First principles and the "human as part of the system" aspects of information visualization from multiple leading sources such as Harvard Business Review, Edward Tufte, and Stephen Few will be explored using representative example data sets. We will discuss best practices for graphical excellence to most effectively, clearly, and efficiently communicate your story. We will construct visualizations for univariate, multivariate, time-dependent, and geographical data. Participants are encouraged to bring laptops to follow along demonstrations in JMP (free trial download at www.jmp.com), and open source solutions such as R (https://www.r-project.org) and Tableau Public (https://public.tableau.com/s/).
Why you should attend:
Data-driven decisions across all regulated industries are now expected. Compliance regulations require analytic solutions that begin with data visualization for discovering relationships and finish with crisp graphs communicating results. As an example, 21 CFR and guidance documents for the pharmaceutical, biopharmaceutical, and medical device industries specify the application of statistical methods for: setting validation criteria and specifications, performing measurement systems analysis (MSA), conducting stability analysis, using design of experiment (DOE) for process development and validation, developing process control charts, and determining process capability indices. Data visualization is the foundation for each one of these areas. In some cases, graphical plots and tables alone may sufficiently address compliance criteria as is the case for the FDA analytical requirements for third-tier critical to quality attributes for analytical biosimilarity evaluations. Data visualization is also essential in other areas such as HIPAA compliance, risk management and analysis, and many other of the quality functions.
Who Will Benefit:
• Data Analysts
• Research Scientists
• Quality Professionals
• Regulatory/Compliance Professionals
• Laboratory Managers
• HR Professionals
• Project Managers
• Design and Development Engineers
• Software Engineers
• Process Owners
• Quality Engineers
• Quality Auditors
• Medical Affairs Professionals
• Process Scientists/Engineers
Agenda:
Day 1 Schedule
Lecture 1:
• Introduction and definitions
• Examples of data visualizations for compliance and regulated industries
• Historical context
• Characteristics of data
• Interactive data visualization exploration with Excel and websites
Lecture 2:
• Human side of data visualization
• Principles of good graphic design
• Data visualization methodology
• Best practices
Lecture 3:
• Software introduction: JMP
• Univariate plots
• Distributions and histograms
• Pie graphs, violin plots, pareto plots, box plots
• Conditional formatting
Lecture 4:
• Mulitvariate plots and heatmaps
• Correlation
• Multivariate scatterplots and density graphs
• Contour plots
• Categorical data plots: treemaps, mosaic plots
Day 2 Schedule
Lecture 1:
• Software introduction: R
• Software introduction: Tableau Public
• Univariate plots with R and Tableau
• Multivariate plots with R and Tableau
Lecture 2:
• Dynamic and interactive graphs
• Brushing, dynamic linking, and filtering
• Profilers on response variables and optimization
Lecture 3:
• Time series plots
• Waterfall plots
• Sparklines and trend lines
• Statistical Process Control charts
Lecture 4:
• Maps
• Text data visualization
• Dashboards
• Course summary
Speaker
James Wisnowski
James Wisnowski is the cofounder of Adsurgo LLC and co-author of the book Design and Analysis of Experiments by Douglas Montgomery: A Supplement for using JMP. He has over 25 years of experience and currently provides training and consulting services to industry and government in Design of Experiments (DOE), Reliability Engineering, Data Visualization, Predictive Analytics, and Text Mining. Dr. Wisnowski has been an invited speaker on applicability of statistics for national and international conferences. Prior to his current position, he was a senior program manager for URS, Chief of the Statistics Division in the Mathematics Department at the Air Force Academy, and a retired military officer. He is currently a member of the editorial board of Quality Engineering and has published numerous international refereed journal articles on statistics. Jim has a PhD in Industrial Engineering from Arizona State University.
Location: Raleigh, NC Date: August 3rd & 4th, 2017 and Time: 9:00 AM to 6:00 PM
Venue: Courtyard Raleigh-Durham Airport 2001 Hospitality Ct, Morrisville, NC 27560, United States
Price:
Register now and save $200. (Early Bird)
Price: $1,295.00 (Seminar Fee for One Delegate)
Until June 20, Early Bird Price: $1,295.00 From June 21 to August 01, Regular Price: $1,495.00
Register for 5 attendees Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)*
Sponsorship Program benefits for “Quality Assurance Auditing for FDA Regulated Industry” seminar
At this seminar, world-renowned FDA Regulated Industry subject matter experts interact with CXO’s of various designations. Executives who carry vast experience about FDA Regulated Industry and Experts get down to discussing industry-related best practices, regulatory updates, changes in technologies, and much more relating to FDA Regulated Industry.
As a sponsor of these seminars, you get the opportunity to have your product and company reach out to C-Level executives in FDA Regulatory -related industries and become known among these elite executives and subject matter experts. Apart from being seen prominently at these globally held seminars, you also get talked about frequently in our correspondences with our experts and these participants.
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