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Changing Regulatory and Reimbursement Scenario for Medical Devices in the US Market
Date:5/21/2013

NEW YORK, May 21, 2013 /PRNewswire/ -- Reportlinker.com announces that a new market research report is available in its catalogue:

 

Changing Regulatory and Reimbursement Scenario for Medical Devices in the US Market

http://www.reportlinker.com/p01188015/Changing-Regulatory-and-Reimbursement-Scenario-for-Medical-Devices-in-the-US-Market.html#utm_source=prnewswire&utm_medium=pr&utm_campaign=Medical_Imaging

 

Changing Regulatory and Reimbursement Scenario for Medical Devices in the US Market

 

Summary

 

GBI Research's report "Changing Regulatory and Reimbursement Scenario for Medical Devices in the US Market" looks at the regulatory landscape and reimbursement scenario in the US for four medical device markets: cardiovascular devices, neurostimulation devices, diagnostic imaging devices and endoscopy devices. The report provides comprehensive information on establishment registration, medical device listing, Premarket Notification (510k) or Premarket Approval (PMA), Investigational Device Exemption (IDE) for clinical studies, Quality System (QS) regulation, labeling requirements, and Medical Device Reporting (MDR). The report also reviews the reimbursement scenario in these medical device markets. It is built using data and information sourced from proprietary databases, primary and secondary research and in-house analysis by GBI Research's team of industry experts.

 

Scope

 

- The report analyzes the regulatory and reimbursement scenario for medical devices in the US.

- Information on the regulatory landscape in the US: establishment registration, medical device listing, Premarket Notification (
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