Russell, Hugo &Amp; Ayliffe's Principles and Practice of Disinfection, Preservation &Amp; Sterilization
DOI: 10.1002/9780470755884.ch21
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Good Manufacturing Practice

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Cited by 3 publications
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“…The final microbiological quality of the finished products together with their antibacterial activities are of clinical significance as comprehensively outlined by the European Pharmacopoeia (EP), the British Pharmacopoeia (BP) and the United States Pharmacopoeia (USP) 3 . Indeed, the industrial manufacturing of the antibiotics principally based on the large scale production of microorganisms, which later convert the corresponding raw materials into the precise antibiotics by a process called fermentation which further undergoes the downstream processing for the recovery of antibiotics [3][4] .…”
Section: Introductionmentioning
confidence: 99%
“…The final microbiological quality of the finished products together with their antibacterial activities are of clinical significance as comprehensively outlined by the European Pharmacopoeia (EP), the British Pharmacopoeia (BP) and the United States Pharmacopoeia (USP) 3 . Indeed, the industrial manufacturing of the antibiotics principally based on the large scale production of microorganisms, which later convert the corresponding raw materials into the precise antibiotics by a process called fermentation which further undergoes the downstream processing for the recovery of antibiotics [3][4] .…”
Section: Introductionmentioning
confidence: 99%
“…The industrial manufacturing of antibiotics is of significant importance in order to maintain the quality of the active ingredients of the antibiotics and additionally, it's really important to set the excipients at appropriate concentrations as per the recommendations and guidelines set by the British Pharmacopoeia (BP) or the European Pharmacopoeia (EP), or the United States Pharmacopoeia (USP) 3 . Moreover, as per the guidelines set by the Food and Drug Administration (FDA) as well as by the standard operating procedures (SOPs) set by the pharmaceutical manufacturing and packaging regulatory guidelines (usually guided both by the FDA and the Pharmacopoeia), the total quality management (TQM) is emphasized through the implementation of the good manufacturing practice (GMP) starting from the raw materials ending up to the finished products ready for distribution into the market for sales [3][4][5] .…”
Section: Introductionmentioning
confidence: 99%