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MEDICAL DEVICES 2010 - Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs - Medical Devices webinar By ComplianceOnline
Website http://complianceonline.com/ecommerce/control/trainingFocus/~product_id=701369?channel=ourglocal |
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Category Medical Devices,conference,event,Webinar
Deadline: December 16, 2010 | Date: December 16, 2010
Venue/Country: Palo Alto, U.S.A
Updated: 2010-12-03 17:58:24 (GMT+9)
Call For Papers - CFP
Why Should You Attend:This webinar is focused on understanding the requirements of the Medical Device Directives, their linkage to the EU Clinical Trial Directive and the requirements of CE Marking and ISO Certification on commercializing products. The course covers all relevant topics in brief associated with the Directives and Guidance Documents, the reasons behind their introduction and a review of methods for effective implementation.Note: Use This PromoCode( 108530 ) To Get 10% Discount valid till Dec 20th.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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