S 3029 · 107th Congress 2001–2003, ended

Patient Safety Improvement and Medical Injury Reduction Act

Fact sheet

Latest action · Oct 2, 2002 Read twice and referred to the Committee on Health, Education, Labor, and Pensions.

Progress

Where this bill reached, and when. A stage with no date was not reached; one that failed a vote and later carried shows the date it carried.

  1. IntroducedOct 2, 2002
  2. Passed SenateNot reached
  3. Passed HouseNot reached
  4. To the PresidentNot reached
  5. Became lawNot reached

Summary

Patient Safety Improvement and Medical Injury Reduction Act - Amends the Public Health Service Act to set forth that, with certain exceptions, patient safety information shall be privileged and confidential and not subject to specified disclosures. Allows health care providers to waive such privileges. Declares that it is unlawful for any person to disclose patient safety information in violation of this Act (with specified exceptions).

Grants protection against adverse employment actions to individuals who report certain types of information to providers or patient safety organizations.

Requires the Director of the Agency for Healthcare Research and Quality to establish: (1) a Center for Quality Improvement and Patient Safety; (2) a National Patient Safety Database; and (3) a National Patient Safety Research Demonstration System.

Requires the Director to approve the process by which a patient safety organization is initially certified and recertified.

Directs the Secretary of Health and Human Services to award grants to eligible entities to promote community partnerships for health care improvement among providers, with the aim of improving the quality of medical care in communities.

Requires the Secretary to develop voluntary, national standards that promote interoperability of health care information technology systems across all health care settings.

Directs the Secretary to appoint a Medical Information Technology Advisory Board.

Allows the Secretary to make grants for: (1) computerized physician order entry systems; (2) informatics systems; and (3) patient safety research.

Amends provisions of the Federal Food, Drug, and Cosmetic Act to classify drugs and biological devices as misbranded unless they include a unique product identifier. Directs the Secretary to issue and periodically revise regulations to require the manufacturer of such a product, or its packager or labeler, to include such information on the packaging.

Cosponsors

Members who signed on, in the order they did.

No cosponsors are on file for this measure.

Actions 3

Everything that happened, newest first.

  1. Oct 2, 2002Introduced in Senate
  2. Oct 2, 2002Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
  3. Oct 2, 2002Sponsor introductory remarks on measure. (CR S9848-9849)

Subjects

Assigned by the Library of Congress. Policy area: Health.

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Everything here is as published by Congress: the summary is the Congressional Research Service's, the action wording is the clerks', and the subjects are the Library of Congress's. How far it got is read from the actions themselves, taking the most recent one of each kind, so a bill that failed a vote and later passed is shown as having passed. Records come from this bill on Congress.gov and govinfo.gov.