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Cleaning Validation In Active
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Guidance on aspects of cleaning validation in active ...
apic.cefic.orgCleaning Validation Guidance 3 1.0 Foreword This document has been prepared by the cleaning validation task force within the active pharmaceutical ingredient committee (APIC) of CEFIC. In recent years the subject of cleaning validation in active pharmaceutical ingredient manufacturing plants has received a large amount of attention from regulators,
Annex 1 : Manufacture of Sterile Products 2 Document map
ec.europa.euProcess validation. 101 102 xii. Preventative maintenance – maintaining equipment, utilities and premises (planned and 103 unplanned maintenance) to a standard that will not add significant risk of contamination. 104 105 xiii. Cleaning and disinfection. 106 107 xiv. Monitoring systems - including an assessment of the feasibility of the ...