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Medical Devices - Complying With 820.250 Statistical Methods
Date :
Place : United States, Fremont
Contact Person:Event Manager
Description:
Overview: In this webinar you will learn how to structure your statistical procedures to ensure compliance, and how to avoid these and how to fully comply with the statistical regulations. Why should you Attend: Two of common 483 and Warning letter items are: Lack of valid statistical rationale Inadequate trending of Quality data Learn how to avoid these and how to fully comply with the statistical regulations Areas Covered in the Session: Important elements for each procedure Valid statistical rational Structuring the procedures to reduce the training burden Deviating from procedures Handling when there is not a procedure Who Will Benefit: Corporate and Division Management Regulatory Management and Personnel Internal Auditors QA/QC Engineers and Management Process Engineers and Management Design Engineer and Management Statisticians Speaker Profile: Wayne Taylor is a leading expert on the application of Statistics to the Medical Device and other FDA regulated industries. His new book Statistical Procedure for the Medical Device Industry sets the standard for applying statistics in compliance with Section §820.250, Statistical Techniques of the Code of Federal Regulations. Event Fee: One Dial-in One Attendee Price: US $150.00 Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: [email protected]Medical Devices - Complying With 820.250 Statistical Methods will be held in Fremont,United States on date 2019-02-04
Deadline for abstracts/proposals : 2nd February 2019
Organized By :Netzealous LLC DBA - Compliance4All
Keynote Speakers :
Venue :Fremont, CA, USA
Check the event website for more details.
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