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Introduction to Process Capability

 
  November 26, 2013  
     
 


Compliance Trainings, Online Webinar
15-01-2014


Description : 

Process capability studies are necessary to evaluate the ability of the process to meet specifications. They determine of the process is on target and if the process spread is acceptable. This talk will cover calculation of process capability indices, impact of sample size, confidence intervals and capability analysis of multi-modal and non-normal data.

This webinar is valuable for understanding how process capability studies can be used to validate and represent your process. Identifying the correct methods and sample size will save time and money.

Areas Covered in the Session :
  • Metrics for Process Control
  • Rational sub-grouping
  • Assessing normality
  • Sample size
  • Dealing with non-normal data
  • Capability for multi-modal populations

Who Will Benefit:
  • Management
  • Research and Development
  • Regulatory Affairs personnel
  • Quality assurance personnel
  • Quality control personnel
  • Auditors and Inspectors
 
 
Organized by: Compliance Trainings
Invited Speakers: SWSteven Walfish is a Principal Statistician at Becton Dickinson (BD) in Franklin Lakes, NJ. Mr. Walfish is responsible for non-clinical statistical support for operations, quality and product development. Prior to joining BD in 2012, Mr. Walfish was a Statistician at GE Healthcare in Waukesha, WI responsible for global statistical support. Prior to joining GE Healthcare, Mr. Walfish had a statistical consulting company that provides statistical analysis and training to the 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.

Mr. Walfish brings over 25 years of industrial expertise in the development and application of statistical methods for solving complex business issues including data collection, analysis and reporting.

Mr. Walfish has been an invited lecturer at Medical Design and Manufacturer (MD&M), Institute of Validation Technology (IVT) and Advanstar conferences. Mr. Walfish has been a speaker at ASQ Division and Section conferences. He is also an editorial board member for BioPharm International, and a regular contributor to the magazine.

Mr. Walfish is the secretary for TAG69, senior member of ASQ, a certified quality engineer and past chair of the Biomedical Division (2006-07). 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.
 
Deadline for Abstracts: 15-01-2014
 
Registration:
Single Live : (For One Participant) $ 249

Corporate Live : (For Max. 10 Participants) $ 899

Recording : (Single REC For One Participant - Unlimited Access for 6 Months) $ 299
E-mail: anita.anzo@compliancetrainings.com
 
   
 
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