Design Verification data and Process Validation 2016

  • Free
  • Published date: October 26, 2016
    • Houston, Texas, United States

Overview:
This 2-day seminar provides a 1-day introduction to the statistical tools used to analyze Design Verification data and Process Validation results. The entire 2nd day is spent on Statistical Process Control and Process Capability Indices. The goal of the 1st day is to help the student understand how to choose statistical methods and sample sizes, and to correctly interpret the results. The goal of the 2nd say is to explain how to monitor a validated production process, using tools that can also help improve product quality.
Why should you attend?
All design and/or manufacturing companies perform design verification and/or process validation studies. A clear understanding of relevant statistical principles and statistical methods ensures that such studies are efficient and accurate. In addition, all validated processes must be monitored to ensure their continued suitability (per the FDA).
The statistical methods used for such activities are easily misused when their fundamental principles are not well understood. Mistakes in usage can lead to new products being launched that should have been kept in R&D; or, conversely, can lead to erroneously deciding to not launch a new product. And failure to monitor production processes accurately can lead to a slow decline in product quality.
This seminar provides a thorough, practical introduction to the relevant statistical methods and principles that will help ensure that outputs from R&D, Product Transfer, Manufacturing Engineering, and Production are consistently of high quality.
Areas Covered in the Session:
• FDA, ISO 9001/13485, and MDD requirements
• Statistically valid rationales for sample sizes
• The interpretation of statistical significance and statistical non-significance
• The impact of normality and non-normality
• Tests of Normality
• Transformations to Normality
• Concepts of "Confidence" and "Reliability" (a.k.a., %-in-specification)
• Concepts of "Quality" and "Variability" and "Process"
• Risk management
Who will benefit:
• QA/QC Supervisor
• Process Engineer
• Manufacturing Engineer
• QC/QC Technician
• Manufacturing Technician
• R&D Engineer
Location: Houston, TX Date: December 8th & 9th, 2016 and Time: 9:00 AM to 6:00 PM

Venue: Courtyard Houston Downtown /Convention Center
Address: 916 Dallas Street Houston Texas 77002 USA Phone: +1 832-366-1600

Price:

Register now and save $200. (Early Bird)

Price: $1,295.00 (Seminar fee for one Delegate Without Stay)

Until October 15, Early Bird Price: $1,295.00 from October 16 to December 6, Regular Price: $1,495.00

Price: $1,695.00 (Seminar fee for one Delegate With Stay)

Until October 15, Early Bird Price: $1,695.00 from October 16 to December 6, Regular Price: $1,895.00

Register for 5 attendees (With stay) Includes Price: $4,323.00 $8,475.00 You Save: $4,152.00 (49%)*

Quick Contact:

NetZealous DBA as GlobalCompliancePanel

Phone: 1-800-447-9407
Fax: 302-288-6884
Email: support@globalcompliancepanel.com
Website: http://www.globalcompliancepanel.com
Registration Link - http://bit.ly/2e8BvgT-Statistical-Methods
Follow us: https://www.linkedin.com/company/globalcompliancepanel

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