Clinical test information access method and device
A technology for clinical trials and information access, applied in the fields of clinical trial information access and computer, to solve problems such as poor information security and leakage of private information
Inactive Publication Date: 2020-12-18
新视焰医疗科技(杭州)有限公司
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Problems solved by technology
[0003] Due to the requirements of the clinical research industry for the protection of subjects and the commitment to the protection of subjects' privacy information in the informed consent document, however, at present, specific personnel in drug clinical trials are checking the information of a certain subject in a certain clinical trial At this time, all the private information of the subject that was consulted was exposed, causing irrelevant personnel other than specific personnel to also be able to browse the subject's private information, resulting in the leakage of the subject's private information, and information security poor
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[0087] Exemplary embodiments of the present application are described below in conjunction with the accompanying drawings, which include various details of the embodiments of the present application to facilitate understanding, and they should be regarded as exemplary only. Accordingly, those of ordinary skill in the art will recognize that various changes and modifications of the embodiments described herein can be made without departing from the scope and spirit of the application. Also, descriptions of well-known functions and constructions are omitted in the following description for clarity and conciseness.
[0088] In a specific embodiment, such as figure 1 As shown, a clinical trial information access method is provided, which is applied to the main server (second server), figure 1 A process in can include the following steps:
[0089] Step S100: Obtain an access instruction of the subject's clinical trial information, the access instruction is sent by the first serve...
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The invention discloses a clinical test information access method and device. According to the specific implementation scheme, the method comprises the steps of obtaining an access instruction of clinical test information of a subject, wherein the access instruction is sent by a first server; calling clinical test information corresponding to the subject according to the access instruction; identifying sensitive information in the clinical test information, and desensitizing the sensitive information to obtain desensitized clinical test information; and sending the desensitized clinical test information to a first server for display. The second server performs desensitization processing on sensitive information in the clinical test information, so that the access security of the clinical test information of the subject is effectively improved. The first server connected with the extranet can protect the second server, so that the second server is prevented from being directly invaded,information in each hospital informatization system connected with the second server is not modified by the extranet, and the security of accessing each hospital informatization system is improved.
Description
technical field [0001] This application relates to the field of computers, in particular to the field of clinical trial information access. Background technique [0002] Drug clinical trials, that is, the discovery or verification of clinical medicine, pharmacology and other pharmacodynamic effects, adverse reactions, or the absorption, distribution, metabolism, and excretion of a certain experimental drug with human subjects before the new drug is marketed, A systematic trial to determine the efficacy and safety of a drug. Drug clinical trials classify patients or healthy persons who enter the trial as "subjects", and subjects who enter the clinical trial sign with the consent of the subjects themselves or their guardians (referred to as "informed consent" in clinical trials) Informed consent, during the clinical trial, the subjects' personal medical information and personal medical information before entering the clinical trial will be allowed to be viewed and processed b...
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IPC IPC(8): G06F21/62G06F21/60G16H10/20G16H10/60
CPCG06F21/604G06F21/6254G06F2221/2141G16H10/20G16H10/60
Inventor 陆益超俞挺娅
Owner 新视焰医疗科技(杭州)有限公司