Browsing Manufacturing Engineering by Subject "Pharmaceutical technology--Quality control"
Now showing items 1-3 of 3
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Applying a Quality Risk Management Approach to a Cleaning Validation System
(Polytechnic University of Puerto Rico, 2014)Cleaning Validation is a crucial step on assuring product effectiveness and safety by assuring that the equipment to be used has the appropriate condition to manufacture a new product without any foreign substances ... -
Design a Predictive Control Model for a CIP System
(Polytechnic University of Puerto Rico, 2014)This document describes the analitical method to define control parameters during a clean in place (CIP) cicle in the pharamaceutical/food industry. The new models of CIP systems comes with many automatic controls and ... -
Reliability of Operators performing the Visual Inspection of Parenteral Drug Products
(Polytechnic University of Puerto Rico, 2010)The visual inspection of parenteral product filled vials is performed to assure that any damaged or defective unit is detected and removed prior to packaging. This investigation evaluated the visual inspection process ...