2015 - Webinar On Better Alternatives to Sampling Plans
Date2015-02-12
Deadline2015-02-12
VenueMississauga, Canada
KeywordsFda Sampling Plans; FDA regulations; Fda ISO 13485 requirements
Topics/Call fo Papers
Description :
The seminar begins with an examination of ISO and FDA regulations and guidelines regarding the use of statistics, especially in regards to Sampling Plans.
The pros and cons of the 2 most widely used sampling plans (ANSI Z1.4, and Squeglia's C=0) are examined in detail, focusing especially on the weaknesses of such plans in regards to meeting regulatory requirements. Real-world examples are provided for how using such sampling plans leads to production of non-conforming product.
The advantages of "confidence/reliability" calculations are explained. Such calculations are demonstrated for Attribute data (pass/fail, yes/no data) as well as for variables data (i.e., measurements). If variables data is "Normally distributed" the calculations are extremely simple. The seminar explains how to handle "non-Normal" data, and provides the methods, formulas, and tools to handle such situations.
The seminar ends with a discussion of how one OEM manufacturer has implemented "confidence/reliability" calculations instead of AQL sampling plans for all of its clients. And suggestions are given for how to use "confidence/reliability" QC specifications instead of "AQL" QC specifications. The use of "reliability plotting" for assessing product reliability during R&D is also discussed.
Areas Covered in the Session :
AQL and LQL sampling plans
OC Curves
AOQL
ANSI Z1.4
Squeglia's C=0
Confidence/Reliability calculations for
Attribute data
Normally-distributed variables data
non-Normal data
Transformations to Normality
K-tables
Normal Probability Plot
Reliability Plotting
Who Will Benefit:
QA/QC Supervisor
Process Engineer
Manufacturing Engineer
QC/QC Technician
Manufacturing Technician
R&D Engineer
Price Tags:
Live
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
For more information and enquiries contact us at
Compliance Trainings
5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Customer Support : 4169154458
Email : support-AT-compliancetrainings.com
The seminar begins with an examination of ISO and FDA regulations and guidelines regarding the use of statistics, especially in regards to Sampling Plans.
The pros and cons of the 2 most widely used sampling plans (ANSI Z1.4, and Squeglia's C=0) are examined in detail, focusing especially on the weaknesses of such plans in regards to meeting regulatory requirements. Real-world examples are provided for how using such sampling plans leads to production of non-conforming product.
The advantages of "confidence/reliability" calculations are explained. Such calculations are demonstrated for Attribute data (pass/fail, yes/no data) as well as for variables data (i.e., measurements). If variables data is "Normally distributed" the calculations are extremely simple. The seminar explains how to handle "non-Normal" data, and provides the methods, formulas, and tools to handle such situations.
The seminar ends with a discussion of how one OEM manufacturer has implemented "confidence/reliability" calculations instead of AQL sampling plans for all of its clients. And suggestions are given for how to use "confidence/reliability" QC specifications instead of "AQL" QC specifications. The use of "reliability plotting" for assessing product reliability during R&D is also discussed.
Areas Covered in the Session :
AQL and LQL sampling plans
OC Curves
AOQL
ANSI Z1.4
Squeglia's C=0
Confidence/Reliability calculations for
Attribute data
Normally-distributed variables data
non-Normal data
Transformations to Normality
K-tables
Normal Probability Plot
Reliability Plotting
Who Will Benefit:
QA/QC Supervisor
Process Engineer
Manufacturing Engineer
QC/QC Technician
Manufacturing Technician
R&D Engineer
Price Tags:
Live
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
For more information and enquiries contact us at
Compliance Trainings
5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Customer Support : 4169154458
Email : support-AT-compliancetrainings.com
Other CFPs
- Webinar On Application of Risk Management in Accordance with EN ISO 14971:2012
- Webinar On Corrective and Preventive Action (CAPA) utilizing the Principles of Lean Documents and Lean Configuration
- Webinar On Performance Appraisal Toolbox: How to Prepare & Deliver Legal & Effective Appraisals
- Webinar On Good Laboratory Practice Regulations - Introduction and Strategies for Implementation
- Webinar On Good Documentation Practices for Clinical Trials
Last modified: 2015-01-15 18:39:30