Sec. 3. Amendment to the Public Health Service Act
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The Public Health Service Act ( 42 U.S.C. 201 et seq. ) is amended by adding at the end the following: In this title: The term abortion means the intentional use or prescription of any instrument, medicine, drug, or any other substance or device or method to terminate the life of an unborn child, or to terminate the pregnancy of a woman known to be pregnant with an intention other than— to produce a live birth and preserve the life and health of the child after live birth; or to remove an ectopic pregnancy, or to remove a dead unborn child who died as the result of a spontaneous abortion, accidental trauma or a criminal assault on the pregnant female or her unborn child.
The term abortion provider means any person legally qualified to perform an abortion under applicable Federal and State laws. The term pain-capable unborn child means an unborn child who has reached a probable stage of development of 20 weeks or more after fertilization. Nothing in subparagraph
(A)shall be construed as a determination or finding by Congress that pain may not in fact be experienced by an unborn child at stages of development prior to 20 weeks or more after fertilization. The term probable age of development means the duration of development after fertilization of the unborn child at the time an abortion is performed, as determined in the good faith judgment of the abortion provider using generally accepted medical criteria and information obtained by interviewing the pregnant woman. The term unborn child means a member of the species homo sapiens, at any stage of development, who is carried in the womb. The term woman means a female human being whether or not she has reached the age of majority. The term unemancipated minor means an individual who is not older than 18 years and who is not emancipated under State law. Any abortion provider in or affecting interstate or foreign commerce, who knowingly performs any abortion of a pain-capable unborn child, shall comply with the requirements of this title. Before any part of an abortion involving a pain-capable unborn child begins, the abortion provider or his or her agent shall provide the pregnant woman involved, by telephone or in person, with the information described in paragraph (2). It may not be provided by a tape recording, but must be provided in a fashion that permits the woman to ask questions of and receive answers from the abortion provider or his agent. (In the case of the Unborn Child Pain Awareness Brochure, it may be provided pursuant to subsection (c)(2) or (c)(3)). An abortion provider or the provider’s agent to whom paragraph
(1)applies shall provide the following information to the pregnant woman (or in the case of a deaf or non-English speaking woman, provide the statement in a manner that she can easily understand): The probable age of development of the unborn baby based on the number of weeks since fertilization. An abortion provider to whom paragraph
(1)applies must provide the pregnant woman with the Unborn Child Pain Awareness Brochure (referred to in this section as the Brochure ) to be developed by the Department of Health and Human Services under subsection
(c)or with the information described in subsection (c)(2) relating to accessing such Brochure. Drugs administered to the mother may not prevent the unborn child from feeling pain, but in some cases, anesthesia or other pain-reducing drug or drugs can be administered directly to the unborn child. After providing the information required under clauses (i), (ii), and
(iii)the abortion provider shall provide the woman involved with his or her best medical judgment on the risks, if any, of administering such anesthesia or analgesic, and the costs associated therewith. If the abortion provider is not qualified or willing to administer the anesthesia or other pain-reducing drug to an unborn child in response to a request from a pregnant women, the provider shall— arrange for a qualified specialist to administer such anesthesia or drug; or advise the pregnant woman— where she may obtain such anesthesia or other pain reducing drugs for the unborn child in the course of an abortion; or that the abortion provider is unable to perform the abortion if the woman requires that she receive anesthesia or other pain-reducing drug for her unborn child. An abortion provider to which paragraph
(1)applies shall provide the pregnant woman with the Unborn Child Pain Awareness Decision Form (provided for under subsection (d)) and obtain the appropriate signature of the woman on such form. Nothing in this section may be construed to impede an abortion provider or the abortion provider’s agent from offering their own evaluation on the capacity of the unborn child to experience pain, the advisability of administering pain-reducing drugs to the unborn child, or any other matter, as long as such provider or agent provides the required information, obtains the woman’s signature on the decision form, and otherwise complies with the affirmative requirements of the law. An abortion provider to whom paragraph
(1)applies shall provide the pregnant woman with the Unborn Child Pain Awareness Brochure (referred to in this section as the Brochure ) to be developed by the Department of Health and Human Services under subsection
(c)or with the information described in subsection (c)(2) relating to accessing such Brochure. An abortion provider to which paragraph
(1)applies shall provide the pregnant woman with the Unborn Child Pain Awareness Decision Form (provided for under subsection (d)) and obtain the appropriate signature of the woman on such form. Not later than 90 days after the date of enactment of this title, the Secretary shall develop an Unborn Child Pain Awareness Brochure. Such Brochure shall— be written in English and Spanish; contain the following text: Your doctor has determined that, in his or her best medial judgment, your unborn child is at least 20 weeks old. There is a significant body of evidence that unborn children at 20 weeks after fertilization have the physical structures necessary to experience pain. There is substantial evidence that at least by this point, unborn children draw away from surgical instruments in a manner which in an infant or an adult would be interpreted as a response to pain. There is substantial evidence that the process of being killed in an abortion will cause the unborn child pain, even though you receive a pain-reducing drug or drugs. Under the Federal ; Unborn Child Pain Awareness Act of 2013 , you have a right to know that there is evidence that the process of being killed in an abortion will cause your unborn child pain. You may request that anesthesia or other pain-reducing drug or drugs are administered directly to the pain-capable unborn child if you so desire. The purpose of administering such drug or drugs would be to reduce or eliminate the capacity of the unborn child to experience pain during the abortion procedure. In some cases, there may be some additional risk to you associated with administering such a drug. contain greater detail on her option of having a pain-reducing drug or drugs administered to the unborn child to reduce the experience of pain by the unborn child during the abortion; be written in an objective and nonjudgmental manner and be printed in a typeface large enough to be clearly legible; and be made available by the Secretary at no cost to any abortion provider. The Brochure under this section shall be available on the Internet website of the Department of Health and Human Services at a minimum resolution of 70 DPI (dots per inch). All pictures appearing on the website shall be a minimum of 200x300 pixels. All letters on the website shall be a minimum of 12 point font. All such information and pictures shall be accessible with an industry standard browser, requiring no additional plug-ins. An abortion provider or his or her agent must provide a pregnant woman with the Brochure, developed under paragraph (1), before any part of an abortion of a pain-capable child begins. The brochure may be provided— through an in-person visit by the pregnant woman; through an e-mail attachment, from the abortion provider or his or her agent; or by certified mail, mailed to the woman at least 72 hours before any part of the abortion begins. After the abortion provider or his or her agent offers to provide a pregnant woman the brochure, a pregnant woman may waive receipt of the brochure under this subsection by signing the waiver form contained in the Unborn Child Pain Awareness Decision Form. Not later than 30 days after the date of enactment of this title, the Secretary shall develop an Unborn Child Pain Awareness Decision Form. To be valid, such form shall— with respect to the pregnant woman— contain a statement that affirms that the woman has received or been offered all of the information required in subsection (b); affirm that the woman has read the following statement: You are considering having an abortion of an unborn child who will have developed, at the time of the abortion, approximately __ weeks after fertilization. There is a significant body of evidence that unborn children at 20 weeks after fertilization have the physical structures necessary to experience pain. There is substantial evidence that at least by this point, unborn children draw away from surgical instruments in a manner which in an infant or an adult would be interpreted as a response to pain. There is substantial evidence that the process of being killed in an abortion will cause the unborn child pain, even though you receive a pain-reducing drug or drugs. Under the Federal ; Unborn Child Pain Awareness Act of 2013 , you have a right to know that there is evidence that the process of being killed in an abortion will cause your unborn child pain. You may request that anesthesia or other pain-reducing drug or drugs are administered directly to the pain-capable unborn child if you so desire. The purpose of administering such drug or drugs would be to reduce or eliminate the capacity of the unborn child to experience pain during the abortion procedure. In some cases, there may be some additional risk to you associated with administering such a drug. require the woman to explicitly either request or refuse the administration of pain-reducing drugs to the unborn child; and be signed by a pregnant woman prior to the performance of an abortion involving a pain-capable unborn child; and with respect to the abortion provider— contain a statement that the provider has provided the woman with all of the information required under subsection (b); if applicable, contain a certification by the provider that an exception described in section 3403 applies and the detailed reasons for such certification; and be signed by the provider prior to the performance of the abortion procedure. The Secretary shall promulgate regulations relating to the period of time during which copies of forms under subsection
(d)shall be maintained by abortion providers. The provisions of section 3402 shall not apply to an abortion provider in the case that the abortion is necessary to save the life of a mother whose life is endangered by a physical disorder, physical illness, or physical injury, including a life-endangering physical condition caused by or arising from the pregnancy itself. An abortion provider who willfully fails to comply with the provisions of this title shall be subject to civil penalties in accordance with this section in an appropriate Federal court. The Attorney General of the United States may commence a civil action under this section. Upon a finding by a court that a respondent in an action commenced under this section has knowingly violated a provision of this title, the court shall notify the appropriate State medical licensing authority and shall assess a civil penalty against the respondent in an amount not to exceed $100,000. Upon a finding by a court that the respondent in an action commenced under this section has knowingly violated a provision of this title and the respondent has been found to have knowingly violated a provision of this title on a prior occasion, the court shall notify the appropriate State medical licensing authority and shall assess a civil penalty against the respondent in an amount not to exceed $250,000. A pregnant woman upon whom an abortion has been performed in violation of this title, or the parent or legal guardian of such a woman if she is an unemancipated minor, may commence a civil action against the abortion provider for any knowing or reckless violation of this title for actual and punitive damages. .
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Sec. 3
Amendment to the Public Health Service Act
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