This webinar covers the statistical methods used to calculate sample sizes for both attribute and variables data. Methods for collecting the sample will be covered. Every sampling plan has risks. This webinar covers how to calculate Type I and Type II errors. A discussion of how the FDA views sampling plans, especially for validation and acceptance activities. Sample size to ensure a certain level of process capability will be covered

Date : 19th February 2015 to 19th February 2015

Place : United States, Fremont

Website :http://www.compliance4all.com/control/webinarsearch?topic_name=&category_id=-1&speaker_id=-1&webinar_month=2

Contact Person:Adam Fleaming

Description:

This webinar covers the statistical methods used to calculate sample sizes for both attribute and variables data. Methods for collecting the sample will be covered. Every sampling plan has risks. This webinar covers how to calculate Type I and Type II errors. A discussion of how the FDA views sampling plans, especially for validation and acceptance activities. Sample size to ensure a certain level of process capability will be covered

This webinar covers the statistical methods used to calculate sample sizes for both attribute and variables data. Methods for collecting the sample will be covered. Every sampling plan has risks. This webinar covers how to calculate Type I and Type II errors. A discussion of how the FDA views sampling plans, especially for validation and acceptance activities. Sample size to ensure a certain level of process capability will be covered will be held in Fremont,United States on date 2015-02-19

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Deadline for abstracts/proposals : 18th February 2015

Keynote Speakers :

Check the event website for more details.