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    MEDICAL DEVICES 2011 - Webinar on Medical Device Tracking - Medical Devices Webinar By ComplianceOnline

    View: 2044

    Website http://complianceonline.com/ecommerce/control/trainingFocus/~product_id=701855?channel=ourglocal | Want to Edit it Edit Freely

    Category Medical Devices,conference,event,Webinar

    Deadline: March 31, 2011 | Date: March 31, 2011

    Venue/Country: Palo Alto, U.S.A

    Updated: 2011-03-11 15:33:30 (GMT+9)

    Call For Papers - CFP

    Why Should You Attend:

    The Food and Drug Administration Modernization Act (FDAMA) requires that manufacturers track certain devices when the agency orders them to do so. Tracking is intended to facilitate notification and recall in the event a device presents a serious risk to health that requires prompt attention. The tracking provisions enacted by SMDA in section 519(e) required mandatory tracking even if FDA did not issue an order.

    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.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.