Jan 31, 2007 | PACS, Patient Safety, Recalls | 0 |
In the next few months, 24×7, as well as two regulatory bodies, will seek your expert opinions. Through November 9, 2006, the FDA is asking for comments about the possible development and implementation of a unique device identifier (UDI) system for medical devices that could reduce medical errors, facilitate device recalls, and improve medical device adverse-event […]
Read MoreJan 31, 2007 | Equipment Disposal | 0 |
These tips will help you assess your equipment and options for the best results
Read MoreJan 31, 2007 | Education, Government Regulations | 0 |
The FDA tests a more comprehensive program for reporting medical-device errors.
Read MoreJan 31, 2007 | Contracts, PACS, Recalls, Ventilators | 0 |
BMETs and clinical engineers are a vital component of the imaging equipment acquisition process.
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