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Prioritizing Cleaning Validation
Pharmaceutical Technology Europe ; 33(6):34-35,40, 2021.
Article in English | ProQuest Central | ID: covidwho-20242754
ABSTRACT
Among the observations noted were failure to maintain clean and sanitary conditions;lack of written procedures for cleaning and decontamination of the vessels used to transport and store materials at the site;and no formal requirements to clean and sanitize these vessels after each use. [...]documentation must include the names and signatures of staff performing the work, as well as the product batch number, cleaner expiry date, and disinfectants used. Single-use systems and equipment have eliminated some of those problems, but they persist for hybrid plants still using stainless steel equipment. More work is also being done to use analytical methods to reduce the subjectivity of visual inspection, but Forsyth hasn't seen any consistentlyin place from the time of marketing authorization application (MAA) filing.
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Collection: Databases of international organizations Database: ProQuest Central Type of study: Observational study / Prognostic study Language: English Journal: Pharmaceutical Technology Europe Year: 2021 Document Type: Article

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Collection: Databases of international organizations Database: ProQuest Central Type of study: Observational study / Prognostic study Language: English Journal: Pharmaceutical Technology Europe Year: 2021 Document Type: Article