Pharma Analytics – I Have All These Data, Now What Do I Do?
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Category Pharma Analytics webinar, pharma data analytics, quality assurance in pharma, Data Pedigree, Validate Prediction Model Accuracy, Pharma Compliance Training
Deadline: March 21, 2017 | Date: March 21, 2017
Venue/Country: New Hyde Park, U.S.A
Updated: 2017-02-21 18:00:35 (GMT+9)
Call For Papers - CFP
Overview:We know that it takes more than a large data set and computer software to effectively solve problems. As information technology increases in capability and availability the opportunity to use data to develop and improve processes becomes even greater. Particular attention is paid to the pedigree of the data: the process that generated the data, the measurement process and the data collection process including the sampling schemes used. Also essential to success is the use of subject matter knowledge to frame the problem and assess and interpret the results of the analysis.Why Should You Attend:The role “Data Analytics” play in Pharma’s Business world todayHow to get started in developing models from dataHow to verify the prediction accuracy over timeTips, Traps and guidelines for conducting successful data analytics studiesAreas Covered in this Webinar:Importance of Data and Analytics in Today’s WorldWhat is Analytics?Developing Models – Getting StartedModel Verification - Developing Models that Predict Accurately over TimeSuccess FactorsWhat We’ve LearnedLearning Objectives:Understand “Building Blocks” of Data AnalyticsHow to Assess Data Quality … “Data Pedigree”Strategic and sequential approach to developing prediction modelsHow to Validate Prediction Model AccuracySuccess Factors for Analytics ProjectsWho Will Benefit:ExecutivesDepartment ManagersQuality EngineersResearch and Development ScientistsBiologists and Microbiologists Chemists and Chemical EngineersProcess and Manufacturing EngineersQuality Assurance PersonnelSupply Chain ProfessionalsAccounting ProfessionalsAnyone with a desire to learn the fundamentals of methodical performance improvementSpeaker Profile:Ronald D. Snee, PhD is Founder and President of Snee Associates, a firm dedicated to the successful implementation of process and organizational improvement initiatives. He provides guidance to senior executives in their pursuit of improved business performance using Quality by Design, Lean Six Sigma and other improvement approaches that produce bottom line results. Prior to his consulting career he spent 24 years at the DuPont Company in a variety of assignments including pharmaceuticals. He has been developing and applying QbD methodologies for more than 30 years. His recent application and research on QbD has produced more than ten articles on use of QbD in Pharma and Biotech. He has also co-authored 2 books on the methods and tools of QbD and speaks regularly at conferences and meetings on the subject. He teaches QbD and related methodologies as an Adjunct Professor at Temple University School of Pharmacy and Rutgers University Pharmaceutical Engineering program.For more detail please click on this below link:http://bit.ly/2lyuImsEmail: referralscomplianceglobal.usToll Free: +1-844-746-4244Tel: +1-516-900-5515Fax: +1-516-900-5510
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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