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    • 1. 发明申请
    • BROADBAND MULTI-CHANNEL DETECTOR WITH SIGNAL AND JAMMING DISCRIMINATION
    • 宽带多通道信道检测器,具有信号和串扰
    • US20080084345A1
    • 2008-04-10
    • US11778992
    • 2007-07-17
    • John RougasStephen McMahonDouglas Owen
    • John RougasStephen McMahonDouglas Owen
    • G01S7/38
    • G01S7/38H04K3/42H04K3/43H04K3/92H04K3/94H04K2203/16H04K2203/24
    • Methods of determining whether a jamming signal strength is adequate, comprising receiving a signal, determining first and second noise power levels of the signal in first and second ranges of frequencies, the first range being broader than and encompassing the second range, and calculating a ratio of the second noise power level divided by the first noise power level. Also, methods of determining whether a jamming signal strength is adequate, comprising receiving a signal, determining a phase difference between first and second frequency range phases of the signal, and calculating a statistical mean and/or a standard deviation of the phase difference. Also, systems for determining whether a jamming signal is adequate, computer-readable media for determining whether jamming signal strength is adequate, systems comprising means for transmitting a jamming signal, and systems comprising means for transmitting and receiving waveforms to users in the presence of protective jamming.
    • 确定干扰信号强度是否足够的方法,包括接收信号,确定所述信号在第一和第二频率范围中的第一和第二噪声功率电平,所述第一范围宽于并包含所述第二范围,并且计算比率 的第二噪声功率电平除以第一噪声功率电平。 此外,确定干扰信号强度是否足够的方法,包括接收信号,确定信号的第一和第二频率范围相位之间的相位差,以及计算相位差的统计平均值和/或标准偏差。 此外,用于确定干扰信号是否足够的系统,用于确定干扰信号强度是否足够的计算机可读介质,包括用于发送干扰信号的装置的系统以及包括用于在存在保护的情况下向用户发送和接收波形的装置的系统 干扰
    • 3. 发明申请
    • System for conducting clinical trials
    • 进行临床试验的系统
    • US20070156459A1
    • 2007-07-05
    • US10536503
    • 2003-11-27
    • Stephen McMahonBruce Neal
    • Stephen McMahonBruce Neal
    • A61B5/00
    • G06Q50/22G06Q10/087G06Q50/24G16H10/20
    • There is disclosed a system (1) for conducting a clinical trial of a pharmaceutical substance on a plurality of trial participants. The system (1) includes a central database (2) having a memory means in communication with a database means, one or more trial sites each having a remote computer (3) located remotely from the central database (2) and in communication therewith, the central database (2) being configured to receive predetermined parameters of the trial, both the central database (2) and the remote computers (3) being configured to receive predetermined trial data from one or more trial participants, the central database (2) being configured to control and track the ordering, allocation and dispensing of the pharmaceutical substances and compiling a pharmaceutical substance inventory record on the central database, and the central database (2) being configured to terminate the clinical trial in response to one or more predetermined trial termination conditions. A method of conducting a clinical trial of a pharmaceutical substance on a plurality of trial participants is also disclosed.
    • 公开了一种用于在多个试验参与者上进行药物物质的临床试验的系统(1)。 系统(1)包括具有与数据库装置通信的存储装置的中央数据库(2),每个具有远离中央数据库(2)并与之通信的远程计算机(3)的一个或多个试用站, 所述中央数据库(2)被配置为接收所述试用的预定参数,所述中央数据库(2)和所述远程计算机(3)被配置为从一个或多个试用参与者接收预定试用数据,所述中央数据库(2) 被配置为控制和跟踪药物物质的排序,分配和分配以及在中央数据库上编制药物物质清单记录,并且中央数据库(2)被配置为响应于一个或多个预定试验终止临床试验 终止条件。 还公开了在多个试验参与者上进行药物物质的临床试验的方法。
    • 6. 发明申请
    • SYSTEM AND METHOD FOR AUTONOMIC BLOOD PRESSURE REGULATION
    • 自动血压调节系统及方法
    • US20140067003A1
    • 2014-03-06
    • US13956344
    • 2013-07-31
    • Abhi VaseStephen McMahon
    • Abhi VaseStephen McMahon
    • A61N1/36A61N1/05
    • A61N1/36117A61B5/0215A61B5/6876A61N1/0551
    • A system for regulating blood pressure by stimulating an afferent pathway to the brain which produces an efferent output in kidneys includes a electrode device adapted for implantation in the cervical region, a stimulator generator, a cable connecting the electrode device and the stimulator generator, wherein the cervical region is generally located between a pair of common carotid arteries, above an aortic arch and in front of cervical vertebrae C2 and C3. A method of implantation includes placing the electrode device in the cervical region, selectively energizing the device in accordance with a stimulation scheme, assessing any changes in the patient's blood pressure, selectively energizing the device in accordance with another stimulation scheme, and assessing any changes in the patient's blood, for determining an optical stimulation scheme, wherein stimulation scheme involves parameters including, for example, position, placement and configuration of the electrode device in relation to surrounding tissue and/or organs, selection of electrodes energized, width, frequency and amplitude of stimulation current.
    • 通过刺激在肾中产生输出输出的通向脑的传入途径来调节血压的系统包括适于植入颈部区域的电极装置,刺激器发生器,连接电极装置和刺激器发生器的电缆,其中, 颈部区域通常位于一对颈总动脉之间,主动脉弓上方和颈椎C2和C3前方。 一种植入方法包括将电极装置放置在颈部区域中,根据刺激方案选择性地激励装置,评估患者血压的任何变化,根据另一刺激方案选择性地激励装置,以及评估任何变化 患者的血液,用于确定光学刺激方案,其中刺激方案涉及包括例如相对于周围组织和/或器官的电极装置的位置,放置和配置的参数,通电选择,宽度,频率和幅度 的刺激电流。