Part of the book series: Monographs in Health Care Administration ((MHCA,volume 2))

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Abstract

Although my topic for discussion is regulation of technology, my own position falls between a laissez faire approach to technology and a direct regulatory approach. I do not believe that market forces and competition alone, without a systematic mechanism for assessing technology and disseminating the findings, will resolve problems of use, distribution and cost inflation. I also do not believe that regulatory approaches such as certificate of need or rate regulation can be rational and effective without such assessments. An organized monitoring and assessment process is necessary.

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References

  1. U.S. Congress, House of Representatives, 95th Congress, 2nd Session, Report #95–1190 by the Committee on Interstate and Foreign Commerce: Health Services Research, Health Statistics and Health Care Technology Act, U.S.G.P.O. 1978, Washington, D.C.

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Authors

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James R. Gay M.D. Barbara J. Sax Jacobs J.D.

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© 1983 Spectrum Publications, Inc.

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Hanft, R.S. (1983). Monitoring Medical Technology: Shall Technology be Regulated? How and by Whom?. In: Gay, J.R., Sax Jacobs, B.J. (eds) The Technology Explosion in Medical Science: Implications for the Health Care Industry and the Public (1981-2001). Monographs in Health Care Administration, vol 2. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-7399-5_9

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  • DOI: https://doi.org/10.1007/978-94-011-7399-5_9

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-011-7401-5

  • Online ISBN: 978-94-011-7399-5

  • eBook Packages: Springer Book Archive

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