Integrity Test for Hepa Filters in Cleanroom Preparation and Cleanroom Process of Labled Compound
نویسندگان
چکیده
منابع مشابه
Integrating Z and Cleanroom
We describe an approach to integrating the Z specification notation into Cleanroom-style specification and verification. In a previous attempt, a group at IBM used formal refinement of the Z in their development. They concluded that this was not cost-effective in a commercial environment, and the attempt was not judged successful. The current approach avoids formal refinement, and instead begin...
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The 'cleanroom software development process is a new IBM technical and organizational approach to developing software with certifiable reliability. Key ideas behind the process are well structured software specifications, randomized testing methods and the, introduction of statistical controls; but the main point is to deny entry for defects during the development of software. This latter point...
متن کاملارزیابی پارامترهای عملکردی در فیلترهای هپا در یک صنعت دارویی(مطالعه موردی1394)
Abstract: Background and aims: Nowadays, cleanrooms have become impartible parts of an industry with sensitive products. Sources of contamination in cleanrooms are impaired performance and quality sensitive products in the cleanrooms .The aim of this study was to evaluate the efficiency of HEPA filter and check the concentration and number of airborne particles in cleanrooms for pharmaceutic...
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ژورنال
عنوان ژورنال: Indonesian Journal of Pharmaceutical Science and Technology
سال: 2019
ISSN: 2406-856X,2356-1971
DOI: 10.24198/ijpst.v1i3.20986