바이오의약 공정의 CIP 시스템 적격성 평가와 사이클의 개선=

Title
바이오의약 공정의 CIP 시스템 적격성 평가와 사이클의 개선=
Authors
도기준
Keywords
CIP
Issue Date
2008
Publisher
인하대학교
Abstract
Cleaning is the most important part of Good Manufacturing Practice (GMP) in the biopharmaceutical industry. It is a mandatory process where the main objective is to avoid contamination across consecutive batches. The Clean-In-Place (CIP) system is a wide
Description
1. Introduction 1 1.1 Importance of Bioprocessing Cleaning 1 1.2 Consideration of the Plant Design 2 1.2.1 Materials 2 1.2.2 Surface Finish 4 1.2.3 Tanks 5 1.2.4 Valves 7 1.2.5 Pumps 8 1.2.6 Utilities 12 1.2.7 Facili
URI
http://dspace.inha.ac.kr/handle/10505/15662
Appears in Collections:
College of Natural Science(자연과학대학) > Ocean Sciences (해양과학) > Theses(해양과학 석박사 학위논문)
Files in This Item:
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