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MEDICAL DEVICES 2011 - The 510(k) Process and Risk Management
Website http://complianceonline.com/ecommerce/control/trainingFocus/~product_id=701497?channel=ourglocal |
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Category Medical Devices,conference,event,Webinar
Deadline: April 15, 2011 | Date: April 15, 2011
Venue/Country: Palo Alto, U.S.A
Updated: 2011-03-11 18:51:11 (GMT+9)
Call For Papers - CFP
Why Should You Attend: The majority of medical devices being placed on the US market are cleared through the Premarket Notification or 510(k) process. Recently FDA has indicated it is tightening this process after some controversy surrounding devices cleared for market. This controversy resulted in replacement of the Director of the Center of Devices and Radiological Devices. An internal report identified some issues and called for an external review of the process, which the FDA commissioned. Manufacturers need to prepare for the impact to product clearance for the US market.NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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