Study and Application of Electronic Records in the Pharmaceutical Equipment

DOI

10.2991/icecee-15.2015.199How to use a DOI?

Keywords

GMP; Wet Granulation; Electronic records; Audit software

Abstract

The drug quality safety is a issue that governments have attached great importance to. The Chinese version of the CMP puts forward strict requirements of " traceability " in the pharmaceutical production process for the pharmaceutical industry.This paper mainly introduces how to realize the electronic record problems and solving method in the production of pharmaceuticals and for automatic control system of wet granulating machine, for meet the "traceability" requirement of the new version of GMP.The electronic record meets the requirements of GMP in pharmaceutical process,so as to ensure the quality of medicines, and achieved good production effect in practical production.

Copyright

© 2015, the Authors. Published by Atlantis Press.

Open Access

This is an open access article distributed under the CC BY-NC license (http://creativecommons.org/licenses/by-nc/4.0/).

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TY  - CONF
AU  - Ning Shi
AU  - Hui Liu
AU  - Yujuan Liu
PY  - 2015/06
DA  - 2015/06
TI  - Study and Application of Electronic Records in the Pharmaceutical Equipment
BT  - Proceedings of the 2015 International Conference on Electrical, Computer Engineering and Electronics
PB  - Atlantis Press
SP  - 1055
EP  - 1060
SN  - 2352-538X
UR  - https://doi.org/10.2991/icecee-15.2015.199
DO  - 10.2991/icecee-15.2015.199
ID  - Shi2015/06
ER  -