Study and Application of Electronic Records in the Pharmaceutical Equipment
Ning Shi, Hui Liu, Yujuan Liu
Available Online June 2015.
- https://doi.org/10.2991/icecee-15.2015.199How to use a DOI?
- GMP; Wet Granulation; Electronic records; Audit software
- 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.
- Open Access
- This is an open access article distributed under the CC BY-NC license.
Cite this article
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 - 2015 2nd 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 - https://doi.org/10.2991/icecee-15.2015.199 ID - Shi2015/06 ER -