The medical device development process has become increasingly complex in recent years. The advent of new technology concepts, stricter regulatory requirements, and the ever increasing importance of reimbursement decisions for successful device commercialization require careful planning and strategy-setting, coordinated decisions, and consistent, rigorous business processes. The design and implementation of such processes, often captured in development models and accompanying standard operating procedures, have become a key determinant of the success of device commercialization. While various models may exist in the device industry, no comprehensive development model has been published. This paper reviews existing model representations and presents a new comprehensive development model that captures all aspects of device development and commercialization from early-concept selection to postmarket surveillance. This model was constructed based on best-practice analysis and in-depth interviews with more than 80 seasoned experts actively involved in the development, commercialization, and regulation of medical devices. The stage-gate process includes the following five phases: (1) initiation - opportunity and risk analysis, (2) formulation - concept and feasibility, (3) design and development - verification and validation, (4) final validation - product launch preparation, and (5) product launch and postlaunch assessment. The study results suggest that stage-gate processes are the predominant development model used in the medical device industry and that regulatory requirements such as the food and drug adminstration (FDA’s) Quality Systems Regulation play a substantive role in shaping activities and decisions in the process. The results also underline the significant differences between medical device innovation and drug discovery and development, and underscore current challenges associated with the successful development of the increasing number of combination products.
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June 2009
Research Papers
Stage-Gate Process for the Development of Medical Devices
Jan B. Pietzsch,
Jan B. Pietzsch
Department of Management Science and Engineering,
Stanford University
, 380 Panama Way, Stanford, CA 94305-4026; Wing Tech Inc.
, 9916 Newhall Road, Potomac, MD 20854
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Lauren A. Shluzas,
Lauren A. Shluzas
Department of Management Science and Engineering, and Department of Mechanical Engineering,
Stanford University
, 380 Panama Way, Stanford, CA 94305-4026
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M. Elisabeth Paté-Cornell,
M. Elisabeth Paté-Cornell
Department of Management Science and Engineering,
Stanford University
, 380 Panama Way, Stanford, CA 94305-4026
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Paul G. Yock,
Paul G. Yock
Department of Bioengineering,
Stanford University
, James H. Clark Center, 318 Campus Drive, E-100, Stanford, CA 94305-5428
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John H. Linehan
John H. Linehan
Department of Bioengineering,
Stanford University
, James H. Clark Center, 318 Campus Drive, E-100, Stanford, CA 94305-5428; Clinical and Translational Sciences Institute, Northwestern University
, 750 North Lake Shore Drive, Chicago, IL 60611
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Jan B. Pietzsch
Department of Management Science and Engineering,
Stanford University
, 380 Panama Way, Stanford, CA 94305-4026; Wing Tech Inc.
, 9916 Newhall Road, Potomac, MD 20854
Lauren A. Shluzas
Department of Management Science and Engineering, and Department of Mechanical Engineering,
Stanford University
, 380 Panama Way, Stanford, CA 94305-4026
M. Elisabeth Paté-Cornell
Department of Management Science and Engineering,
Stanford University
, 380 Panama Way, Stanford, CA 94305-4026
Paul G. Yock
Department of Bioengineering,
Stanford University
, James H. Clark Center, 318 Campus Drive, E-100, Stanford, CA 94305-5428
John H. Linehan
Department of Bioengineering,
Stanford University
, James H. Clark Center, 318 Campus Drive, E-100, Stanford, CA 94305-5428; Clinical and Translational Sciences Institute, Northwestern University
, 750 North Lake Shore Drive, Chicago, IL 60611J. Med. Devices. Jun 2009, 3(2): 021004 (15 pages)
Published Online: June 17, 2009
Article history
Received:
May 12, 2008
Revised:
May 3, 2009
Published:
June 17, 2009
Citation
Pietzsch, J. B., Shluzas, L. A., Paté-Cornell, M. E., Yock, P. G., and Linehan, J. H. (June 17, 2009). "Stage-Gate Process for the Development of Medical Devices." ASME. J. Med. Devices. June 2009; 3(2): 021004. https://doi.org/10.1115/1.3148836
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