公开(公告)号：US08635047B2

公开(公告)日：2014-01-21

申请号：US12312852

申请日：2007-11-30

申请人： Hélène Desjobert ,  Jean Podvin

发明人： Hélène Desjobert ,  Jean Podvin

IPC分类号： G06F11/30

CPC分类号： G01N35/00871 ,  G06F19/00 ,  G06F19/3418 ,  G16H40/40

摘要： A method of inspecting point-of-care biological test appliances by means of an inspection appliance comprises the steps of: receiving qualitative data characterizing the test appliance and the environment in which the appliance is found; receiving the value of a control solution as measured by the test appliance; acquiring the value of the control solution as measured by a reference appliance; transmitting the test value, the reference value, and the qualitative data to a centralizing computer system; determining a bias expected between the received test value and the acquired reference value; comparing the test value with the reference value while taking the bias into account to obtain comparison data; storing the comparison data in association with the qualitative data; generating an inspection report within the computer system; and sending the report to the inspection appliance or to a computer terminal associated with the inspection appliance.

摘要翻译： 通过检查设备检查生物检测点的方法包括以下步骤：接收表征测试仪器和找到该设备的环境的定性数据; 接收由测试仪器测量的控制解决方案的值; 获取由参考设备测量的控制解决方案的值; 将测试值，参考值和定性数据发送到集中式计算机系统; 确定在所接收的测试值与所获取的参考值之间预期的偏差; 将测试值与参考值进行比较，同时考虑偏差以获得比较数据; 存储与定性数据相关联的比较数据; 在计算机系统内生成检查报告; 并将报告发送到检查设备或与检查设备相关联的计算机终端。

公开(公告)号：US20100131239A1

公开(公告)日：2010-05-27

申请号：US12312852

申请日：2007-11-30

申请人： Hélène Desjobert ,  Jean Podvin

发明人： Hélène Desjobert ,  Jean Podvin

IPC分类号： G06F19/00 ,  G08B21/00

CPC分类号： G01N35/00871 ,  G06F19/00 ,  G06F19/3418 ,  G16H40/40

摘要： The invention relates to a method of inspecting point-of-care biological test appliances (i=10 to 14) for on-site implementation from an “inspection” appliance (2). According to the invention, the method comprises the steps of: a) on-site inputting or reception (E1) of qualitative data (QLD[i]) characterizing a point-of-care biological test appliance (i) for inspection and characterizing the environment in which the appliance is to be found; b) on-site inputting or reception (E0) of the value (QTD[i]) of a biological variable of a “control” solution (SC) as measured by the point-of-care biological test appliance (i) for inspection; c) acquiring (E2) the value (QTD[i]) of the biological variable of the control solution (SC) as measured by a reference biological test appliance (3); d) transmitting (E3) the input or received value (QTD[i]), the acquired value (QTDCTL), and the input or received qualitative data (QLD[i]) to a centralizing computer system (4); e) within the centralizing computer system (4), determining (E4) a bias (B[i]) that is to be expected between the input or received value (QTD[i]) of the biological variable and the value (QTDCTL) as measured by the reference appliance (3), the expected bias being determined as a function of the input or received qualitative data (QLD[i]), including data relating to the environment in which the appliance is used, and of comparison data (DC) stored in the computer system (4); f) comparing (E5) the value (QTD[i]) as measured by the point-of-care biological test appliance with the value (QTDCTL) as measured by the reference appliance (3) while taking the bias (B[i]) into account; g) storing (E6) comparison data (DC) relating to the comparison performed in the computer system (4), said comparison data being stored in association with the qualitative data; h) within the computer system, generating a inspection report (C-R); and i) sending (E7) the report (C-R) to the inspection appliance (2, 3′) or to a computer terminal associated with the inspection appliance (2, 3′).