FDA Inspection and Respond to 483 & How to Prepare them - 2017
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Website http://www.compliance4all.com/control/w_product/~product_id=501362LIVE?channel=ourglocal_Aug_2017_SE |
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Category 2017 FDA Inspection, Warning Letters, Form 483 Webinars, compliance online 2017 trainings, FDA form 483 programs, Quality Management, Manufacturing Management courses, compliance software trainings
Deadline: August 07, 2017 | Date: August 08, 2017
Venue/Country: Online, U.S.A
Updated: 2017-06-15 15:11:58 (GMT+9)
Call For Papers - CFP
Overview:In this webinar you will learn about the types of FDA inspections, preparations such as assigning dedicated personnel to specific tasks for the inspection, facility requirements to support the inspection.Why should you Attend: FDA is required to conduct an inspection every two years. A company that is prepared for the inspection is less likely to receive 483's than a disorganized company. If a 483 is received knowing how to respond will lessen chances of receiving a Warning Letter. Areas Covered in the Session:Personnel PreparationFacility needed to support inspectionBehavior during inspection-what not to signInternal/ Mock audits483 responseWho Will Benefit:Engineering PersonnelEngineering ManagementQuality ManagementCorporate ManagementManufacturing ManagementDivision ManagementSpeaker Profile:Edwin Waldbusser is a consultant retired from industry after 20 years in management of development of medical devices (5 patents). He has been consulting in the US and internationally in the areas of design control, risk analysis and software validation for the past 8 years.Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: supportcompliance4All.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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