Drug clinical trial monitoring method and system based on block chain, device and medium

A clinical trial and monitoring system technology, applied in drug reference, special data processing applications, instruments, etc., can solve the problems of high data storage space overhead, to achieve the effect of ensuring authenticity and reliability, solving high data storage space overhead, and protecting rights and interests

Inactive Publication Date: 2018-12-21
INST OF SOFTWARE APPL TECH GUANGZHOU & CHINESE ACAD OF SCI
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  • Abstract
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Problems solved by technology

[0018] Aiming at the grinding problem of complex die-casting parts, the present invention provides a blockchain-based drug clinical trial monitoring method, system, equipment and medium to realize the protection of the rights and interests of subjects, ensure the authenticity and reliability of data, and solve the problem of data storage in existing systems Defects such as large space overhead

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  • Drug clinical trial monitoring method and system based on block chain, device and medium
  • Drug clinical trial monitoring method and system based on block chain, device and medium
  • Drug clinical trial monitoring method and system based on block chain, device and medium

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Embodiment Construction

[0059] The following will clearly and completely describe the technical solutions in the embodiments of the present invention with reference to the accompanying drawings in the embodiments of the present invention. Obviously, the described embodiments are only part of the embodiments of the present invention, not all of them. Based on the embodiments of the present invention, all other embodiments obtained by persons of ordinary skill in the art without creative efforts fall within the protection scope of the present invention.

[0060] It should be noted that if there is a directional indication (such as up, down, left, right, front, back...) in the embodiment of the present invention, the directional indication is only used to explain the position in a certain posture (as shown in the accompanying drawing). If the specific posture changes, the directional indication will also change accordingly.

[0061] In addition, if there are descriptions involving "first", "second" and ...

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Abstract

The invention discloses a drug clinical trial monitoring method and system based on the block chain, a device and a medium and relates to the technical field of the drug clinical trial. The block chain technology is introduced, test records are maintained jointly by participants in the drug trial and stored in a block chain in a chronological order through the chain structure, through use of the block chain, characteristics can be only added and are non-tamperable and deleteable, and data authenticity and validity are guaranteed; rights of subjects are better protected through the intelligentcontract technology, an informed consent is stored in the block chain in the form of an intelligent contract, during the test, the physiological data of the subjects are obtained in real time throughdocking with the medical device, once the event triggering a contract suspension clause is monitored, payment is automatically executed according to the contract terms; through the decentralized storage idea, defects including large cost of data storage space, incomplete privacy protection and weak anti-attack ability existing in a centralized drug test management system in the prior art are solved.

Description

technical field [0001] The invention relates to the technical field of drug clinical trials, in particular to a block chain-based drug clinical trial monitoring method, system, equipment and media. Background technique [0002] Drug clinical trials refer to the systematic research of drugs in human body to confirm or discover the effects, adverse reactions and / or absorption, distribution, metabolism and excretion of test drugs, with the purpose of determining the efficacy and safety of test drugs sex. The process of drug clinical trials can be briefly summarized into three stages: design, implementation and summary. In 1999, the State Food and Drug Administration promulgated the "Clinical Practice for Drugs", which was revised in 2003 and renamed "Good Clinical Practice for Drugs" (GCP). Clinical trials in my country's Good Clinical Practice (GCP) mainly involve four personnel, including investigators, sponsors (contract research organizations, clinical monitors), ethics c...

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): G16H10/60G16H15/00G16H70/40G06F17/30
CPCG16H10/60G16H15/00G16H70/40
Inventor 袁敏夫李引袁峰
Owner INST OF SOFTWARE APPL TECH GUANGZHOU & CHINESE ACAD OF SCI
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