Upload
john-robinson
View
2
Download
1
Embed Size (px)
DESCRIPTION
The 2-day seminar begins with an examination of ISO and FDA regulations and guidelines regarding the use of statistics. Basic vocabulary and concepts are then reviewed and discussed.
Citation preview
SPEAKER
GlobalCompliancePanel
2-day In-person Seminar:
www.globalcompliancepanel.com All rights are reserved GlobalCompliancePanel.
Knowledge, a Way Forward
Applied Statistics for QA, QC, Manufacturing, and Design Control
John N. Zorich Statistical Consultant & Trainer, Ohlone College & SV Polytechnic
John N. Zorich, has spent 35 years in the medical device manufacturing industry; the rst 20 years were as a "regular" employee in the
areas of R&D, Manufacturing, QA/QC, and Regulatory; the last 15 years were as consultant in the areas of QA/QC and Statistics. His
consulting clients in the area of statistics have included numerous start-ups as well as large corporations such as Boston Scientic,
Novellus, and Siemens Medical. His experience as an instructor in statistics includes having given 3-day workshop/seminars for the past
several years at Ohlone College (San Jose CA).
OVERVIEW
John N. Zorich
July 9th & 10th, 2015
SFO, CA
9.00 AM to 6.00 PM
How to calculate condence intervals (for proportions and for measurements), including a discussion of how to choose sample size
How to perform an interpret t-Tests, including consideration of "signicance", "p-values", "power" and sample-size considerations
How to perform calculation of condence/reliability for attribute data
How to perform calculation of condence/reliability for Normally-distributed variables (measurement) data, including a discussion of how
to choose sample size
How to assess Normality and how to "transform" non-normal data into Normality so that they can be used with Normal K-tables
Course "Applied Statistics for QA, QC, Manufacturing, and
Design Control" has been pre-approved by as eligible for RAPS
up to credits towards a participant's RAC recertication upon 12
full completion.
AGENDA
WHY SHOULD YOU ATTEND
WHO WILL BENEFIT
GlobalCompliancePanel
www.globalcompliancepanel.com All rights are reserved GlobalCompliancePanel.
Knowledge, a Way Forward
DAY ONE DAY TWO
Lecture 1: Regulatory Requirements
Lecture 2: Vocabulary and Concepts
Lecture 3: Condence Intervals (attribute and variables data)
Lecture 4: t-Tests and related "power" estimations
Lecture 5: Condence/Reliability calculations for Proportions
Lecture 6: Condence/Reliability calculations for Normally distributed
data (K-tables)
Lecture 7: Normality Tests and Normality Transformations
Lecture 8: Reliability Plotting (e.g., for non-normal data and/or
censored studies)
Lecture 9: Statistical Analysis of Gages (introduction to Gage R&R,
Gage Correlation, etc.)
Lecture 10: QC Sampling Plans (attribute AQL plans, and alternatives
to such plans)
Lecture 11: Statistical Process Control (introduction, with focus on
XbarR charts)
Lecture 12: Process Capability Indices calculations(Cp, Cpk, Pp, Ppk)
Lecture 13: Implementation Recommendations
Almost all design and/or manufacturing companies evaluate product and processes either to establish product/process specications, to QC to such
specications, and/or to monitor compliance to such specications.
The various statistical methods used to support such activities can be intimidating to master. If used incorrectly, such methods can result in new products
being launched that should have been kept in R&D; or, conversely, deciding to not launch a new product because of incorrectly calculated product reliability
or process capability. In QC, mistakenly chosen sample sizes and inappropriate statistical methods may result product being rejected that should have
passed, and vice-versa.
This seminar provides a practical approach to understanding how to interpret and use a standard tool-box of statistical methods, including condence
intervals, t-tests, Normal K-tables, Normality tests, condence/reliability calculations, AQL sampling plans, measurement equipment analysis, and Statistical
Process Control. Without a clear understanding and correct implementation of such methods, a company risks signicantly increasing its complaint rates,
scrap rates, and time-to-market; and signicantly reducing its product and service quality, its customer satisfaction levels, and its prot margins.
QA/QC Supervisor
Process Engineer
Manufacturing Engineer
QC/QC Technician
Manufacturing Technician
R&D Engineer
GlobalCompliancePanel
www.globalcompliancepanel.com All rights are reserved GlobalCompliancePanel.
Knowledge, a Way Forward
1. Learning Objectives
2. Participation certificates
3. Interactive sessions with the US expert
4. Post event email assistance to your queries.
5. Special price on future purchase of web based trainings.
6. Special price on future consulting or expertise services.
7. Special price on future seminars by
GlobalCompliancePanel.
8. Seminar Kit includes presentation handout, ID card,
brochure, trainings catalog, notepad and pen.
9. Networking with industry's top notch professionals
What you get
Credit Card: Use the Link to make Payment by
Visa/Master/American Express card click on the register
now link
Check: Kindly make the check payable to NetZealous DBA
GlobalCompliancePanel and mailed to 161 Mission Falls
Lane, Suite 216, Fremont, CA 94539, USA
PO: Please drop an email to
[email protected] or call the our toll
free +1-800-447-9407 for the invoice and you may fax the
PO to 302 288 6884
Wire Transfer: Please drop an email to
[email protected] or call our toll free
+1-800-447-9407 for the wire transfer information
Payment Options:
Get fabulous discounts by participating in groups of two or more.
Price for One Delegate pass Price: $1,695.00
Register now and save(Early Bird) (Early Bird) Price $200.
Pricing List
**Please note the registration will be closed 2 days (48 Hours) prior to
the date of the seminar.
Group participations
AttendeesNo Discount
1 2 Attendees
2 3 to 6 Attendees
3 7 to 10 Attendees
4 10+ Attendees
10% off
20% off
25% off
30% off
Register Here