Creating Optimal Sampling Plans

The purpose of this webinar is to present to the listener the importance of creating a statistically based sampling plan and, how to present those in viable protocols.

Yuval Shapiro
Instructor:
Yuval Shapiro
Date:
Wednesday, September 25, 2019
Time:
10:00 AM PDT | 01:00 PM EDT
Duration:
60 Minutes

More Trainings by this Expert   Product Id : 502723

Price Details
$150 Live
$290 Corporate Live
$190 Recorded
$390 Corporate Recorded
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Live + Recorded
$289 $340 Live + Recorded
Corporate (Live + Recorded)
$599 $680 Corporate
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Overview:

A sampling plan is a term widely used in research studies that provide an outline on the basis which of research is conducted. It tells which category is to be surveyed, what should be the sample size and how the respondents should be chosen out of the population.

The purpose of this webinar is to present to the listener the importance of creating a statistically based sampling plan and, how to present those in viable protocols.

Why should you Attend: Verification and validation protocols (i.e. - Design verification protocols, design validation protocols, production process verification, etc.). This webinar will provide the basic understanding:

  • The basic statistical requirements
  • When a sampling plan is required
  • How to construct a Sampling Plan

Areas Covered in the Session:
  • Basic Statistical Terms: Population, samples and descriptors
  • Sample plans for design verification
  • Sample plans for process validation

Who Will Benefit:
  • Engineers


Speaker Profile
Yuval Shapiro is the founder of QWV - Quality with Value, QA or RA Services. An expert for products and companies primarily related to medical devices that meet the real needs of their clientele. Substantial experience gained in various multi-discipline technology industries (Military, Telecom & Medical Devices), and give a high value contribution to quality and reliability projects related to the medical device and telecom industries.

More than 20 years of experience in QA; including MD and D RA and QA; QMS (21CFR - Part820, ISO13485, TL9000, CMDCAS, ISO9001). More than 20 years of experience in QA; including MD&D RA & QA; QMS (21CFR - Part820, ISO13485, TL9000, CMDCAS, ISO9001). EH and S Systems; QA or RA representative in R and D Projects. Risk Analysis as per ISO14791 & ISO31000. EMC & Safety Certifications.




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