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Statistical Methods A Visual Approach 2017

Start Date:
Thursday, 3 August, 2017
End Date:
Friday, 4 August, 2017 6:00pm
Speciality:
Infectious Disease, Internal Medicine, Emergency Medicine, Pulmonary Medicine, Family Practice, Physical Medicine, Headache / Migraine, Health & Nutrition
Website:
http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901114SEMINAR?meetings4docs-August-2017-SEO

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 AnalystsResearch ScientistsQuality ProfessionalsRegulatory/Compliance ProfessionalsLaboratory ManagersHR ProfessionalsProject ManagersDesign and Development EngineersSoftware EngineersProcess OwnersQuality EngineersQuality AuditorsMedical Affairs ProfessionalsProcess Scientists/Engineers Agenda: Day 1 Schedule Lecture 1:Introduction and definitionsExamples of data visualizations for compliance and regulated industriesHistorical contextCharacteristics of dataInteractive data visualization exploration with Excel and websites Lecture 2:Human side of data visualizationPrinciples of good graphic designData visualization methodologyBest practices Lecture 3:Software introduction: JMPUnivariate plotsDistributions and histogramsPie graphs, violin plots, pareto plots, box plotsConditional formatting Lecture 4:Mulitvariate plots and heatmapsCorrelationMultivariate scatterplots and density graphsContour plotsCategorical data plots: treemaps, mosaic plots Day 2 Schedule Lecture 1:Software introduction: RSoftware introduction: Tableau PublicUnivariate plots with R and TableauMultivariate plots with R and Tableau Lecture 2:Dynamic and interactive graphsBrushing, dynamic linking, and filteringProfilers on response variables and optimization Lecture 3:Time series plotsWaterfall plotsSparklines and trend linesStatistical Process Control charts Lecture 4:MapsText data visualizationDashboardsCourse summary SpeakerJames 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: $1,495.00Register 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" seminarAt 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. For More Information- https://www.globalcompliancepanel.com/control/sponsorship Normal 0 false false false EN-US X-NONE X-NONE /* Style Definitions */ table.MsoNormalTable{mso-style-name:"Table Normal";mso-tstyle-rowband-size:0;mso-tstyle-colband-size:0;mso-style-noshow:yes;mso-style-priority:99;mso-style-parent:"";mso-padding-alt:0in 5.4pt 0in 5.4pt;mso-para-margin-top:0in;mso-para-margin-right:0in;mso-para-margin-bottom:10.0pt;mso-para-margin-left:0in;line-height:115%;mso-pagination:widow-orphan;font-size:11.0pt;font-family:"Calibri","sans-serif";mso-ascii-font-family:Calibri;mso-ascii-theme-font:minor-latin;mso-hansi-font-family:Calibri;mso-hansi-theme-font:minor-latin;}

Location

Courtyard Raleigh-Durham Airport 2001 Hospitality Ct,
Morrisville,
North Carolina,
27560,
United States

Organizer Details

Conference organized by NetZealous DBA as GlobalCompliancePanel

Address:
NetZealous LLC-globalcompliancepanel, 161 Mission Falls Lane, Suite 216, Fremont,CA94539, USA
Phone:
Event Manager
Email:
john.robinson@globalcompliancepanel.com

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