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  4. Architectural Planning for Biomedical Pharmaceutical Factory
 
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Architectural Planning for Biomedical Pharmaceutical Factory

Date Issued
2006
Date
2006
Author(s)
Yu, Wen-Li
DOI
zh-TW
URI
http://ntur.lib.ntu.edu.tw//handle/246246/50489
Abstract
The subject of this study is「Biomedical Pharmaceutical Factory」which is categorized to high-danger character. In accordance with domestic and foreign related cGMP and Biological Safety Level III, its vaccine explains concept and methodology of safety design toward requirement and guidance of space, environment, circulation, air-conditioning, mechanical and electrical engineering and instrumental facilities. To utilize interview of specialist with fairly experience and to present its actual case, basic research of planning have been undertaken. In order to open a new theme for architectural domain, reference for coming planning is expected. Due to time restriction, 「Biomedical Pharmaceutical Factory」 and related topic will be in-depth analyzed only with planning layer. The main analysis includes seven items of its planning of circulation, partition, air-conditioning, electricity system, alarm and monitor system, water supply/drainage and sewage system as well as instrumental facilities. Through discussing with experts and scholars in all aspects, besides the whole collection and analysis laws and norms, a practical planning to「Biomedical Pharmaceutical Factory」 has been undertaken. The basic study of seven planning are: creature safety area, peace and quiet, in- and out-circulation of personnel, circulation of material (clean, polluted), in- and out-circulation of pharmaceutical preparation (cell/germs/virus fungus, original material, sampling, cultivate buffer fluid, product, injection bottle, intermedium), the move-off circulation of discard, as well as pressure flow direction. In the light of planning of「Biomedical Pharmaceutical Factory」, improvement and suggestion have been established in order to refine its current insufficient planning and reference afterward. The results will be helpful to improve its shortage of specialized planning, as well as to promote of attaching importance and planning level. Establishing of improvement to refine its current shortage of planning for afterward is also attempted by this study.
Subjects
生物製劑先導工廠
生物安全第三等級實驗室
cGMP
Biomedical Pharmaceutical Factory
Laboratory of Biological Safety Level III
SDGs

[SDGs]SDG3

[SDGs]SDG16

Type
thesis
File(s)
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Name

ntu-95-R93521714-1.pdf

Size

23.31 KB

Format

Adobe PDF

Checksum

(MD5):303359bcaf739d2c6b8efc0c09329bfe

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