Drug management method and system in trial drug clinical test process

A technology of clinical trials and management methods, applied in the field of drug management, can solve problems such as low drug deployment efficiency, achieve the effects of improving drug deployment efficiency, preventing inaccurate data, and preventing environmental pollution

Pending Publication Date: 2021-12-31
SOOCHOW UNIV AFFILIATED CHILDRENS HOSPITAL
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  • Abstract
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  • Application Information

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Problems solved by technology

[0004] The present invention provides a drug management method and system in the process of trial drug clinical trials, which are used to solve the problem of low efficiency of drug deployment in the existing drug management system:

Method used

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  • Drug management method and system in trial drug clinical test process
  • Drug management method and system in trial drug clinical test process
  • Drug management method and system in trial drug clinical test process

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Embodiment Construction

[0072] The preferred embodiments of the present invention will be described below in conjunction with the accompanying drawings. It should be understood that the preferred embodiments described here are only used to illustrate and explain the present invention, and are not intended to limit the present invention.

[0073] The present invention proposes a drug management method in the trial drug clinical trial process, such as figure 1 As shown, the drug management method includes:

[0074] S1. According to the clinical trial plan of the trial drug, obtain the number of people assigned to each clinical trial center and hospital and the actual distribution of the corresponding trial drug, and distribute the actual distribution of the clinical trial center and hospital, the number of people in the trial, and the corresponding trial drug Quantities are integrated into a clinical trial checklist;

[0075] S2. Send the clinical trial list to the drug delivery department, and the drug...

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Abstract

The invention provides a drug management method and system in a clinical test process of trial drugs. The method comprises the following steps: acquiring the number of distributed testers and the actual distribution amount of corresponding test drugs according to a clinical test plan of the test drugs; sending the clinical test lists to a medicine delivery department, and enabling the medicine delivery department to distribute medicine to the corresponding clinical test centers and hospitals according to the sequence of the clinical test lists; after receiving the medicine, enabling the clinical test center and the hospital to feed back the medicine amount of the received medicine; according to the amount of the received medicine fed back by the clinical test center and the hospital and the actual dispensing amount of the corresponding test medicine on the clinical test list, determining whether medicine dispensing treatment needs to be carried out or not; and monitoring the drug stock in clinical use in real time, and supplying test drugs for clinical test centers and hospitals of which the drug stock is smaller than a preset threshold value of the stock required by the test. The system comprises modules corresponding to the steps of the method.

Description

technical field [0001] The invention provides a drug management method and system in the process of trial drug clinical trials, belonging to the technical field of drug management. Background technique [0002] Clinical trials are a complex experimental system involving many aspects such as pathology, pharmacology, ethics, and statistics. Clinical trials refer to any systematic study of drugs in humans (patients or healthy volunteers) to confirm or reveal the effects, adverse reactions and / or absorption, distribution, metabolism and excretion of test drugs, with the purpose of determining the Drug efficacy and safety. The core of the drug clinical trial is to develop around the experimental drug. In order to ensure that the experimental drug is dedicated to the clinical trial subjects, the supply, use, storage and disposal of the remaining drug are in compliance with the Good Clinical Practice (GCP) Regulation. [0003] At present, in the process of managing the drugs to ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): G16H10/20G16H40/20
CPCG16H10/20G16H40/20
Inventor 蒋云周丽芳薛进柳仁凤余紫初
Owner SOOCHOW UNIV AFFILIATED CHILDRENS HOSPITAL
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