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ISA Trans ; 41(2): 245-54, 2002 Apr.
Article in English | MEDLINE | ID: mdl-12071257

ABSTRACT

This paper describes a case study of a control system design for a batch pharmaceutical process. The ISA standard S88.01 batch control models and terminology were used as the main guidelines for the implementation. As the S88 is not a guide for how to apply the definitions/structures, etc., one of the main goals of our work was to create a methodology for decomposition of functional requirements in terms of S88 models and structures. This methodology was tested on a real problem, described in the case study. Also presented are some remarks on project methodology and Food and Drug Administration validation.


Subject(s)
Computer-Aided Design , Models, Theoretical , Software , Technology, Pharmaceutical/methods , Technology, Pharmaceutical/standards , Crystallization , Czech Republic , Feedback , Filtration/methods , Nystatin/isolation & purification , Quality Control , Technology, Pharmaceutical/instrumentation
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