FDA Inspections - Do's and Don'ts 2019
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Website https://www.compliance4all.com/control/w_product/~product_id=502277LIVE?channel=ourglocal_Mar_2019_S |
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Category senior management, Regulatory management, QA management
Deadline: March 21, 2019 | Date: March 22, 2019
Venue/Country: Online, U.S.A
Updated: 2019-01-21 15:14:27 (GMT+9)
Call For Papers - CFP
Overview:In this webinar speaker will define the steps necessary to prepare for an FDA inspection and discuss details surrounding the management of inspections from announcement to close out meeting.Why should you Attend:This session will discuss how to prepare for the inspection, what to do during the inspection and the close-out interview, and how to respond to the inspection.Areas Covered in the Session:How to prepare for an FDA inspectionDevelopment and contents of an SOP for FDA inspectionPersonnel training before inspectionHow to behave during an inspectionLimitations of scope of inspectionResponse to investigation findingsWho Will Benefit:Executive/senior managementRegulatory managementQA managementAny personnel who may have direct interaction with FDA officialsConsultantsQuality system auditorsSpeaker Profile:Jeff Kasoff , RAC, CMQ/OE is the Principal Consultant at Lean to Quality, LLC. He s has more than 30 years of experience in Quality and Regulatory management. Over that time, He has implemented and overseen quality system operations and assured compliance, at all sizes of company, from start-up to more than $100 million in revenue.Event Fee: One Dial-in One Attendee Price: US$150.00Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: compliance4all14gmail.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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