Manufacturing Expert System Development Guidelines in a Medical Device Manufacturing Company

dc.contributor.advisorNieves Castro, Rafael A.
dc.contributor.authorRivera Rodríguez, Luis A.
dc.date.accessioned2020-10-28T11:28:42Z
dc.date.available2020-10-28T11:28:42Z
dc.date.issued2012
dc.descriptionDesign Project Article for the Graduate Programs at Polytechnic University of Puerto Ricoen_US
dc.description.abstractAbstract - The medical device manufacturing company as well as other regulated industries can only perform manufacturing activities in a strictly controlled environment working area controlled by complex systems that combines pumps, chillers, valves, several types of sensors devices, etc. The tightly integration of those individual components including proper equipment maintenance requires workforce personnel with knowledge in several technical areas of expertise. Recent advancement in computational system capabilities have allowed to develop very complex software programs capable of storing a huge amount of information and later analyze the information to identify patterns, relationships or repetitive events. An expert system is a software solution that has been implemented in different fields like; medicine, law and accounting, to reduce the time to perform troubleshooting and diagnostic. This article presents development guidelines to implement an expert system capable of reducing the business downtime caused by failures in the air handling and chilled water system. Key Terms - Air Handling and Chilled Water System (AHU/CWS), Expert Systems, Inference Engine, Rules.en_US
dc.identifier.citationRivera Rodríguez, L. A. (2012). Manufacturing expert system development guidelines in a medical device manufacturing company [Unpublished manuscript]. Graduate School, Polytechnic University of Puerto Rico.en_US
dc.identifier.urihttp://hdl.handle.net/20.500.12475/918
dc.language.isoenen_US
dc.publisherPolytechnic University of Puerto Ricoen_US
dc.relation.haspartSan Juanen_US
dc.relation.ispartofManufacturing Engineering;
dc.relation.ispartofseriesFall-2012;
dc.rights.holderPolytechnic University of Puerto Rico, Graduate Schoolen_US
dc.rights.licenseAll rights reserveden_US
dc.subject.lcshMedical instruments and apparatus industry--Quality controlen_US
dc.subject.lcshManufacturing processes--Quality controlen_US
dc.subject.lcshMedical instruments and apparatus industry--Managementen_US
dc.subject.lcshPolytechnic University of Puerto Rico--Graduate students--Research
dc.titleManufacturing Expert System Development Guidelines in a Medical Device Manufacturing Companyen_US
dc.typeArticleen_US

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