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H.R. 2589, The Improving Pharmaceuticals for Children Act of 2007

  • This item is from the 110th Congress (2007-2008) and is no longer current. Comments, voting, and wiki editing have been disabled, and the cost/savings estimate has been frozen.

Comparing original version (created by webmaster) with revision saved on August 28, 2007, 18:14:23 (webmaster):

H.R. 2589 would amend the Federal Food, Drug, and Cosmetic Act and the Public Health Service Act to reauthorize and amend the Best Pharmaceuticals for Children Act and the Pediatric Research Equity Act.

== Detailed Summary ==

<summary>
(Log inImproving Pharmaceuticals for Children Act of 2007 - Amends the Federal Food, Drug, and Cosmetic Act to editrevise provisions relating to market exclusivity for pediatric drug studies on new or already approved drugs to: (1) require that appropriate labeling changes are timely made; and (2) prohibit the wikiSecretary of Health and Human Services from extending the period of market exclusivity later than one year prior to the expiration of such period.

Directs the Secretary to: (1) publish a notice identifying any drug for which a pediatric formulation was developed, studied, and found to
be safe and effective in the firstpediatric population if such formulation is not introduced onto the market within one year; and (2) order the labeling of a drug to provideinclude information about the results of a detailed summarypediatric study.

Requires the Secretary, acting through the Director
of the bill!)National Institutes of Heath (NIH), to develop, publish, and revise a priority list of needs in pediatric therapeutics.

Revises requirements for the submission of pediatric assessments of the safety and effectiveness of a drug or biological product with a new drug or supplemental application to require an applicant seeking: (1) a deferral of such requirements to submit a timeline for the completion of such studies; and (2) a waiver of such requirements to submit documentation detailing why a pediatric formulation cannot be developed.

Considers a supplement to any new drug or biological license application proposing a labeling change as a result of any pediatric assessment to be a priority application or supplement.

Requires the Comptroller General to study the effectiveness of federal law in ensuring that medicines used by children are tested and properly labeled.<br>

</summary>

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== Status of the Legislation ==

<status>
Latest Major Action: 6/6/2007: Referred to House committee. Status: Referred to the House Committee on Energy and Commerce.
</status>

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== Points in Favor ==

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== Points Against ==

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