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    Online webinar Sampling Plan for Quality Audits

    View: 213

    Website https://compliance2go.com/product/?pid=CP2014-438 | Want to Edit it Edit Freely

    Category Medical Device

    Deadline: April 19, 2015 | Date: April 20, 2015

    Venue/Country: Online, U.S.A

    Updated: 2015-03-25 16:26:51 (GMT+9)

    Call For Papers - CFP

    DESCRIPTION

    Quality audits typically involve sampling of records and other documents. When the auditor does this, many questions arise, such as how many records to sample and how many nonconforming records are too many. In fact, there is a more fundamental question about nonconforming records. If a record has, say, three errors does the auditor count it three time (once for each error) or one time as a nonconforming record. Some auditors determine the sample size without using statistical techniques. Is this ever acceptable? Sampling records in an audit is not the same as sampling at incoming inspection; the underlying assumptions are different, so the methods need to change.

    Areas covered in the seminar:

    The concepts of sampling when conducting quality audits

    The difference between a nonconformance and nonconformities

    The use of (non-statistical) convenience samples

    Using standard sampling plans in an audit

    Using the binomial distribution to understand audit sampling

    An examination of the FDA’s QSIT sampling plans

    Who will benefit:

    Quality Managers

    Audit Managers

    Lead Quality Auditors

    Quality Auditors

    Regulatory Affairs Managers

    Why you should attend:

    This session examines the issues in audit sampling and provides the answers you need to plan your audit. Participants learn the difference between counting nonconformities and counting nonconformances and which techniques to apply in a quality audit. An audit may need to determine the error rate in a process, or least show that it is not too great. Participants will learn some standard sampling plans as well the reason they work. As an example, participants will analyze the sampling plans the FDA uses as part of the Quality System Technique (QSIT).

    Webinar includes:

    An explanation of how to perform the calculations in Excel

    Q/A Session with the Expert to ask your question

    PDF print only copy of PowerPoint slides

    90 Minutes Live Presentation

    Certificate of attendance


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.