第2部分：用于监管评估的医用显示器的临床前评估。
Part 2: Pre-Clinical Assessment of Medical Displays for Regulatory Evaluation.
作者信息
Badano Aldo, Cheng Wei-Chung, O'Leary Brendan J, Myers Kyle J
机构信息
Center for Devices and Radiological Health, U.S. Food and Drug Administration, 10903 New Hampshire Ave., Bldg 62, Room 3116, Silver Spring, MD 20993; telephone 301/796-2534.
出版信息
Inf Disp (1975). 2011 Apr;27(4):28-31.
Challenges are emerging with regard to the pre-clinical, regulatory assessment of display systems used for viewing and interpreting medical images. This article discusses those, and also the types of evidence that might be relevant to the evaluation of mobile image-viewing devices, true-color devices with applications in digital microscopy, and 3-D medical displays as discussed in Part 1.
在用于查看和解读医学图像的显示系统的临床前监管评估方面，挑战正在浮现。本文将讨论这些挑战，以及与第1部分中所讨论的移动图像查看设备、在数字显微镜中有应用的真彩色设备和3D医学显示器的评估可能相关的证据类型。
Zotero 插件