Massachusetts Institute of Technology
Augmenting drug process development capacity through applications of lean principles and high throughput technology
Abstract
dc:description.abstractThe long development lead time and high R&D costs for biologics drugs makes it imperative to eliminate delays and inefficiencies. Limited process development capacity can lead to delays in the availability of life-saving drugs and a large opportunity cost for biopharmaceutical companies. This study investigates the combined viability and impact of two approaches, namely applying lean principles and using high-throughput technology to increase capacity and productivity in pivotal biologics drug process development. Specifically, the project will explore a framework for improved handoffs and work design, and propose management systems to sustain implementation. In parallel, the study tests the sensitivity of the process development cycle to various resource constraints through a discrete event simulation and develops heuristics for the effective use of high-throughput equipment in upstream and downstream processes to increase process development capacity. The two approaches identified a potential increase in throughput of 2.75X (+175%) in preparation for an anticipated 2.3X (+129%) growth in biologics program demand in pivotal process development.
Degree
thesis:*- Department dc:contributor.department
- Leaders for Global Operations Program at MIT
- Grantor dc:publisher
- Massachusetts Institute of Technology
- Year dc:date.issued
- 2018
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Rustia, Maria Dominique Bautista
- Advisor dc:contributor.advisor
-
- Richard Braatz and Nelson Repenning.
Subjects
dc:subject × 3Rights
dc:rights- Statement dc:rights
-
- MIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission.
- Licence dc:rights.uri
- Language dc:language.iso
- eng
Identifiers
dc:identifier.*- Handle dc:identifier.uri
- http://hdl.handle.net/1721.1/117952
- OAI identifier oai:identifier
- oai:dspace.mit.edu:1721.1/117952