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MEDICAL DEVICES 2011 - Anatomy of a Medical Device Inspection: From EIR to 483 to Warning Letter - Medical Devices webinar By ComplianceOnline
Website http://complianceonline.com/ecommerce/control/trainingFocus/~product_id=701787?channel=ourglocal |
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Category Medical Devices,conference,event,Webinar
Deadline: January 25, 2011 | Date: January 25, 2011
Venue/Country: Palo Alto, U.S.A
Updated: 2010-12-03 18:12:14 (GMT+9)
Call For Papers - CFP
This Medical device inspection webinar training will teach you A to Z of inspection starting with how to prepare to what to do during inspection, close-out interview, FDA’s scope, what documents to show and how to respond to the inspection.Areas Covered in the Seminar:How to prepare for an FDA inspection.Development and contents of an SOP for FDA inspection.Personnel training before inspection.How to behave during an inspection.Limitations of scope of inspection.Response to investigation findings.FDA guidance documents used by their inspectors.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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