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Reed Smith Health Care Reform Review: The Affordable Care Act – Analysis and Implications for Drug, Device and Biotech Manufacturers

By Elizabeth B. Carder-Thompson, Joseph W. Metro, Kevin Madagan, Carol Loepere & Debra A. McCurdy on June 24, 2010
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This post was also written by Robert J. Hill and Jennifer A. Goldstein.

In April 2010, Reed Smith provided an extensive analysis of the recently-enacted health reform legislation, H.R. 3590, the Patient Protection and Affordable Care Act (PPACA), as amended by H.R. 4872, the Health Care and Education Reconciliation Act of 2010 (Reconciliation Act). In this analysis, we concentrate on those provisions in the new law that will affect life sciences entities: pharmaceutical, device, and biologics manufacturers. To read the full alert, click here.

Photo of Elizabeth B. Carder-Thompson Elizabeth B. Carder-Thompson
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  • Posted in:
    Health Care and Life Sciences
  • Blog:
    Life Sciences Legal Update
  • Organization:
    Reed Smith LLP
  • Article: View Original Source

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