Creating Optimal Sampling Plans
July 8, 2020
10:00 AM PDT | 01:00 PM EDT
More Trainings by this Expert
Product Id : 503221
Live: One Dial-in One Attendee
Corporate Live: Any number of participants
Recorded: Access recorded version, only for one participant unlimited viewing for 6 months ( Access information will be emailed 24 hours after the completion of live webinar)
Corporate Recorded: Access recorded version, Any number of participants unlimited viewing for 6 months ( Access information will be emailed 24 hours after the completion of live webinar)
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:
Areas Covered in the Session:
- The basic statistical requirements
- When a sampling plan is required
- How to construct a Sampling Plan
Who Will Benefit:
- Basic Statistical Terms: Population, samples and descriptors
- Sample plans for design verification
- Sample plans for process validation
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.