H.R.5629 - Pathway for Biosimilars Act110th Congress (2007-2008)
|Sponsor:||Rep. Eshoo, Anna G. [D-CA-14] (Introduced 03/13/2008)|
|Committees:||House - Energy and Commerce; Judiciary|
|Latest Action:||04/14/2008 Referred to the Subcommittee on Courts, the Internet, and Intellectual Property.|
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Summary: H.R.5629 — 110th Congress (2007-2008)All Bill Information (Except Text)
Introduced in House (03/13/2008)
Pathway for Biosimilars Act - Amends the Public Health Service Act to allow a person to submit an application for licensure of a biological product based on its similarity to a licensed biological product (the reference product).
Requires the Secretary of Health and Human Services to approve the application if: (1) the biological product is biosimilar to the reference product with respect to each condition of use for which the reference product is approved; and (2) the applicant consents to the inspection of the facility that is the subject of the application.
Sets forth requirements for a determination by the Secretary that a biological product is interchangeable with a reference product.
Prohibits a biological product from being evaluated against more than one reference product.
Prohibits licensure under this Act of a biological product containing specified agents or toxins.
Prohibits the Secretary from making approval of an application under this Act effective until 12 yeas after the date on which the reference product was first licensed.
Provides for confidentiality of information received pursuant to this Act.
Sets forth provisions governing patent infringement actions related to this Act.
Deems as patent infringement the submission of a statement under this Act by the applicant setting forth reasons why the making, use, or sale of the biosimilar product would not infringe the patent, or why the patent is invalid or unenforceable, if the purpose of such submission is to obtain approval to engage in the commercial manufacture, use, or sale before the expiration of such patent.