ListarManufacturing Competitiveness por tema "Pharmaceutical technology--Quality control"
Mostrando ítems 1-4 de 4
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Are cleaning faults, really, quality or administrative issues?: Cleaning Validation Program optimization for a Pharmaceutical plant
(Polytechnic University of Puerto Rico, 2008)The cleaning procedure process validation has generated considerable discussion when executing a US Food and Drug Administration (FDA) inspection at Pharmaceutical Plants. In general, the FDA requires the equipment to be ... -
Cleaning Validation of a Manufacturing Line using CIP-100 Detergent and a Clean-in-place Skid System
(Polytechnic University of Puerto Rico, 2022)Cleaning Validation is a prime element of control to the cross contamination and potential carry over topic at the manufacturing industry. This process must assure the quality, safety and efficiency of cleaning ... -
Inventario y 5s en un Laboratorio de Control de Calidad
(Polytechnic University of Puerto Rico, 2022)Un laboratorio de control de calidad de una farmacéutica es el encargado de asegurar la calidad del producto que allí es manufacturado. Por medio de esta investigación se busca implementar la metodología de 5S y de ... -
Quality Risk Management (QRM) Considerations for Introduction of New Products
(Polytechnic University of Puerto Rico, 2015)Quality Risk Management (QRM) is an optional tool to improve product effectiveness and safety by assuring that the recognized risk is at a desired level. Also risk management tools provide a methodology to evaluate ...