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dc.contributor.advisorStanley B. Gershwin and Andreas S. Schulz.en_US
dc.contributor.authorHill, Brent A. (Brent Alan)en_US
dc.contributor.otherLeaders for Manufacturing Program.en_US
dc.date.accessioned2008-12-11T18:34:50Z
dc.date.available2008-12-11T18:34:50Z
dc.date.copyright2008en_US
dc.date.issued2008en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/43830
dc.descriptionIncludes bibliographical references (p. 89-90).en_US
dc.descriptionThesis (M.B.A.)--Massachusetts Institute of Technology, Sloan School of Management; and, (S.M.)--Massachusetts Institute of Technology, Dept. of Mechanical Engineering; in conjunction with the Leaders for Manufacturing Program at MIT, 2008.en_US
dc.description.abstract(cont.) A multi-criteria objective function uses the researcher's preference to optimize both room assignments and procedure start time. A Tabu search meta-heuristic has been developed to generate a near-optimal solution. The solution approach uses four neighborhood move strategies based on insert and interval exchange algorithms to optimize procedural room assignments. Although a functioning model was not developed, a recommended implementation plan is discussed.en_US
dc.description.abstractThe pharmaceutical industry is experiencing significant competitive pressures. Innovation productivity continues to decline, while the costs for drug R&D steadily rise. This project, sponsored by Novartis Institutes for BioMedical Research (NIBR), is intended to lower drug R&D costs and increase R&D process efficiency through improved research operations. This analysis focuses on improving the scheduling and coordination of early stage, in vivo drug discovery research projects within NIBR's animal facilities. Many of the communication processes used to coordinate research activities in these facilities use ad hoc methods for relaying critical information between research teams and the operations staff. Greater efficiencies can be achieved with the application of risk pooling concepts where dispersed research activities are brought together under a consolidated management structure. These efficiencies cannot be realized until the communication processes are improved. Integral to this improvement effort is the development of a fair and robust method for allocating in vivo resources to research projects using a centralized scheduling system. This thesis provides the framework for developing a centralized scheduling system. The architecture of this tool requires a web-based interface in order to provide seamless access to the research community. Based on research workflows, the proposed tool coordinates input from scientists and uses this information to schedule the required resources. The complex constraints found in a research animal facility dictate the need for a unique scheduling approach. Adapted from existing airline gate scheduling research, this problem is formulated as a mixed integer linear program.en_US
dc.description.statementofresponsibilityby Brent A. Hill.en_US
dc.format.extent98 p.en_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsM.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectMechanical Engineering.en_US
dc.subjectSloan School of Management.en_US
dc.subjectLeaders for Manufacturing Program.en_US
dc.titleIn vivo research scheduling and coordination in the pharmaceutical industryen_US
dc.typeThesisen_US
dc.description.degreeS.M.en_US
dc.description.degreeM.B.A.en_US
dc.contributor.departmentLeaders for Manufacturing Program at MITen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineering
dc.contributor.departmentSloan School of Management
dc.identifier.oclc262694253en_US


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