Discussion on Intelligent File Management System in Pharmaceutical 4.0

DENG Ting; LIU Meng; WU Xiao-yun; HU Rong; ZHENG Xiao-hong

doi:10.13422/j.cnki.syfjx.2018010186

您当前的位置：

首页 >

文章列表页 >

Discussion on Intelligent File Management System in Pharmaceutical 4.0

更新时间：2024-01-04

- Discussion on Intelligent File Management System in Pharmaceutical 4.0
- Chinese Journal of Experimental Traditional Medical Formulae Vol. 24, Issue 1, Pages: 186-190(2018)
- 作者机构：
- 作者简介：
- 基金信息：
- DOI：10.13422/j.cnki.syfjx.2018010186
  CLC： R95;TP315
- Published：2018
- 稿件说明：
移动端阅览
DENG Ting, LIU Meng, WU Xiao-yun, et al. Discussion on Intelligent File Management System in Pharmaceutical 4.0[J]. Chinese journal of experimental traditional medical formulae, 2018, 24(1): 186-190.
DOI：

DENG Ting, LIU Meng, WU Xiao-yun, et al. Discussion on Intelligent File Management System in Pharmaceutical 4.0[J]. Chinese journal of experimental traditional medical formulae, 2018, 24(1): 186-190. DOI： 10.13422/j.cnki.syfjx.2018010186.

摘要

本文以药品生产企业为例，探讨智慧文件管理系统的定义、需求，再结合国内外制药行业药品生产质量管理规范（GMP）检查缺陷项目现状和数据完整性的要求，以数据的4W（who，when，where，what）属性为基础，探讨智慧化文件系统的构建思路，通过3个设计的运用举例来展现该系统具备搜索和逻辑运算功能的显著特点，并预见该系统的优点和实施难点。该系统将有利于制药4.0背景下的工厂实现高效、便捷地利用各类文件进行信息检索和逻辑运算，使得药品研发和注册工作更加科学、系统、有序，同时也利于国际标准化录入和建立绿色低碳、信息化、智能化、国际化的制药核心技术平台。

Abstract

Firstly

the authors took pharmaceutical production enterprises as an example to discuss the definition and requirements of intelligent file management system

and then combined with the domestic and international status of good manufacture practices(GMP) inspection defects in the pharmaceutical industry and the requirements of data integrity

the construction idea of intelligent file system was investigated based on the 4W(who

when

where

what) attribute of data.This paper also showed the characteristics of this system with searching and logical operation functions through the three designed examples.Finally

the advantages and implementation difficulties of the system were foreseen.The system will benefit the factory under the background of pharmaceutical 4.0 to achieve efficient and convenient use of all kinds of documents for information retrieval and logic operations

it will promote the drug research and registration work to be more scientific and systematic

but also be conducive to the international standard input and the establishment of pharmaceutical core technology platform.

关键词

Keywords

references

Views

下载量

CSCD

Alert me when the article has been cited

提交

Tools

Publicity Resources

No data

Related Author

No data

Related Institution

No data

AI问答

Postal code：100700
Tel：010-84076882 Email：syfjx_2010@188.com
Technical support is provided by Beijing Founder electronics co., LTD 京ICP备11006657号-10 京公网安备11010802024621
It is recommended to read the content of this site in Chrome&IE9+. Please switch to extreme mode in browser 360.
Cookies We use cookies to help provide and enhance our service and tailor content. By continuing, you agree to the use of cookies.

⁰