Standardising, Manufacture And Control Of Neo-Sensitabs*
作者:
PedersenO. Gylling,
期刊:
Acta Clinica Belgica
(Taylor Available online 1973)
卷期:
Volume 28,
issue 3
页码: 139-149
ISSN:1784-3286
年代: 1973
DOI:10.1080/17843286.1973.11716866
出版商: Taylor&Francis
数据来源: Taylor
摘要:
SummaryThe reasons why the attainable serum concentration is the principal criterium for standardising Neo-Sensitabs are given, and at the same time details are shown of the interpretation of inhibition-zone readings. The elaborate co-operation between production department and control laboratory in the manufacturing process is described, and subsequently results from stability checks, performed by a microbiological method and by a chemical extraction method, are presented.
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