ListarManufacturing Engineering por tema "Medical instruments and apparatus industry--Quality control"
Mostrando ítems 21-29 de 29
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Quality Improvement in a Medical Device Manufacturing Process Applying Six Sigma Tools
(Polytechnic University of Puerto Rico, 2009)Abstract - The current manufacturing process of a medical device product has great opportunities on scrap percent reduction, which has been impacting the material and labor costs of the product, as well as in defects per ... -
Quality Improvement Process for Software Controls in Regulated Industry using Six Sigma Methodology
(Polytechnic University of Puerto Rico, 2013)A regulated industry at medical devices company, Software Control practices on Automated Processes are weak and not systematized. Several findings were found in past internal audits related to software revision changes. ... -
Reduction of Cosmetic Defects Due to Criteria Misalignment at a Medical Device Manufacturing Line Using DMAIC Methodology
(2013)For the last few years, the economy of Puerto Rico has been negatively affected, increasing the operational cost of the industries in the Island. The Pharma / Medical Device industry is not excluded of this situation. ... -
A Strategically Systematic Approach to Acquire Improvement Project Prospects in a Medical Device Company
(Polytechnic University of Puerto Rico, 2012)Abstract - Numerous companies begin their manufacturing improvement journey lacking an overall game plan. This results in a not strategized and structured improvement implementation with results less than optimal and if ... -
Surgical Technologies Clean Room Lines Capacity Improvement
(Polytechnic University of Puerto Rico, 2015)In today’s competitive market, medical device manufacturing companies need to continuously innovate their products and process in order to maintain a leader position on the medical devices industry. Quality and Cost ... -
Tracking System for Useful Life of an Insulin Pump Motor
(Polytechnic University of Puerto Rico, 2016)This research project was focused in the implementation of a Tracking System for the useful life of an infusion pump’s motor. This component is a sub-assembly of the infusion pump which is used to deliver fluids into ... -
Validation Machine Process of “Crosslink, Low Profile Break-off” On Tornos Deco 20
(Polytechnic University of Puerto Rico, 2016)The United States (U.S.) medical device manufacturing sector is a highly diversified industry that produces a range of products designed to diagnose and treat patients in healthcare systems worldwide. Process validation is ... -
Validation of a New Procedure for a Pacemaker Component
(Polytechnic University of Puerto Rico, 2012)Abstract - Company X manufactures pacemakers in Puerto Rico. Over the past years, Company X has been having a significant amount of complaints due to the septum component contained in its pacemakers. Doctors have claimed ... -
Workmanship Error at Assembly Line in a Medical Device Company
(Polytechnic University of Puerto Rico, 2012)Abstract — In a Medical Device Company a production line had an increase of non-conformances in 2011. The category for the increase was workmanship error. These failures result in cost of poor quality due to quality holds. ...