Applied Statistics, with Emphasis on Verification, Validation, and Risk Management(get 50% off)

  • 2000.00 Dollar US$
  • Published date: February 15, 2019
    • Houston, Houston, United States

Course "Applied Statistics, with Emphasis on Verification, Validation, and Risk Management, in R&D, Manufacturing, and QA/QC" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.
Description:
The 2-day seminar explains how to apply statistics to manage risks and verify/validate processes in R&D, QA/QC, and Manufacturing, with examples derived mainly from the medical device design/manufacturing industry. The flow of topics over the 2 days is as follows:
• ISO standards and FDA/MDD regulations regarding the use of statistics.
• Basic vocabulary and concepts, including distributions such as binomial, hypergeometric, and Normal, and transformations into Normality.
• Statistical Process Control
• Statistical methods for Design Verification
• Statistical methods for Product/Process Qualification
• Metrology: QC Sampling Plans the statistical analysis of measurement uncertainty, and how it is used to establish QC specifications
• How to craft "statistically valid conclusion statements" (e.g., for reports)
Why should you attend:
Almost all design and/or manufacturing companies evaluate product and processes either to manage risks, to validate processes, to establish product/process specifications, to QC to such specifications, and/or to monitor compliance to such specifications.
The various statistical methods used to support such activities can be intimidating. If used incorrectly or inappropriately, statistical methods can result in new products being launched that should have been kept in R&D; or, conversely, new products not being launched that, if analyzed correctly, would have met all requirements. In QC, mistakenly chosen sample sizes and inappropriate statistical methods may result in purchased product being rejected that should have passed, and vice-versa.
Areas Covered in the Session:
• FDA, ISO 9001/13485, and MDD requirements related to statistical methods
• How to apply statistical methods to manage product-related risks to patient, doctor, and the designing/manufacturing company
• Design Control processes (verification, validation, risk management, design input)
• QA/QC processes (sampling plans, monitoring of validated processes, setting of QC specifications, evaluation of measurement equipment)
• Manufacturing processes (process validation, equipment qualification)
Who Will Benefit:
• QA/QC Supervisor
• Process Engineer
• Manufacturing Engineer
• QC/QC Technician
• Manufacturing Technician
• R&D Engineer


Location: Houston, TX Date: March 26th & 27th, 2019 and Time: 9:00 AM to 6:00 PM
Venue: Homewood Suites by Hilton Houston-Kingwood Parc, 23320 Hwy 59 N. Kingwood, TX 77339

Price:
Register for 1 attendees Price: $2,000.00
Register for 5 attendees Price: $10,000.00
Register for 10 attendees Price: $20,000.00
Until February 28, Early Bird Price: $2,000. From March 01 to March 24, Regular Price: $2,200.
use this promo code GCP50 to get 50% off.

Sponsorship Program benefits for seminar
For More Information- https://www.globalcompliancepanel.com/control/sponsorship

Contact us today!
NetZealous LLC DBA GlobalCompliancePanel
globalcompliancepanel@gmail.com
Toll free: +1-800-447-9407
Phone: +1-510-584-9661
Website: http://www.globalcompliancepanel.com

Registration Link - https://www.globalcompliancepanel.com/seminar/applied-statistics-with-emphasis-verification-901933SEMINAR?seo
Follow us on LinkedIn: https://www.linkedin.com/company/globalcompliancepanel/
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