Share Your Research, Maximize Your Social Impacts
Main Menu
Searching By
PARTNERS
Medical Devices 2011 - Webinar on Medical Device Tracking - Medical Devices Webinar By ComplianceOnline
Date2011-03-31
Deadline2011-03-31
VenuePalo Alto, USA - United States 
KeywordsMedical Devices,conference,event,Webinar
Topics/Call fo Papers
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.
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.
Other CFPs
- Medical Device Complaints Handling Strategies for Managing Your Biggest Compliance Challenge
- Assessing FDA’s Proposed Changes to the 510(k) Process in 2011 - Medical Devices Webinar By ComplianceOnline Webinar By ComplianceOnline
- How to Deal with the IRS and other Governmental Agencies - HR Webinar By ComplianceOnline
- Workplace Hostility: Myths and Realities - HR Webinar By ComplianceOnline
- Form W-4: Best Practices for Efficiency, Customer Service and Compliance - HR Webinar By ComplianceOnline
Last modified: 2011-03-11 15:33:30