Transparency reports
Payments or other transfers of value
In general
Special rule for certain payments or other transfers of value
In the case where an applicable manufacturer provides a payment or other transfer of value to an entity or individual at the request of or designated on behalf of a covered recipient, the applicable manufacturer shall disclose that payment or other transfer of value under the name of the covered recipient.
Physician ownership
Penalties for noncompliance
Failure to report
In general
section 1320a–7a of this titleSubject to subparagraph (B) except as provided in paragraph (2), any applicable manufacturer or applicable group purchasing organization that fails to submit information required under subsection (a) in a timely manner in accordance with rules or regulations promulgated to carry out such subsection, shall be subject to a civil money penalty of not less than $1,000, but not more than $10,000, for each payment or other transfer of value or ownership or investment interest not reported as required under such subsection. Such penalty shall be imposed and collected in the same manner as civil money penalties under subsection (a) of are imposed and collected under that section.
Limitation
The total amount of civil money penalties imposed under subparagraph (A) with respect to each annual submission of information under subsection (a) by an applicable manufacturer or applicable group purchasing organization shall not exceed $150,000.
Knowing failure to report
In general
section 1320a–7a of this titleSubject to subparagraph (B), any applicable manufacturer or applicable group purchasing organization that knowingly fails to submit information required under subsection (a) in a timely manner in accordance with rules or regulations promulgated to carry out such subsection, shall be subject to a civil money penalty of not less than $10,000, but not more than $100,000, for each payment or other transfer of value or ownership or investment interest not reported as required under such subsection. Such penalty shall be imposed and collected in the same manner as civil money penalties under subsection (a) of are imposed and collected under that section.
Limitation
The total amount of civil money penalties imposed under subparagraph (A) with respect to each annual submission of information under subsection (a) by an applicable manufacturer or applicable group purchasing organization shall not exceed $1,000,000.
Use of funds
Funds collected by the Secretary as a result of the imposition of a civil money penalty under this subsection shall be used to carry out this section.
Procedures for submission of information and public availability
In general
Establishment
Definition of terms
The procedures established under subparagraph (A) shall provide for the definition of terms (other than those terms defined in subsection (e)), as appropriate, for purposes of this section.
Public availability
Clarification of time period for review and corrections
In no case may the 45-day period for review and submission of corrections to information under subparagraph (C)(ix) prevent such information from being made available to the public in accordance with the dates described in the matter preceding clause (i) in subparagraph (C).
Delayed publication for payments made pursuant to product research or development agreements and clinical investigations
In general
Confidentiality of information prior to publication
section 552 of title 5Information described in clause (i) shall be considered confidential and shall not be subject to disclosure under or any other similar Federal, State, or local law, until on or after the date on which the information is made available to the public under such clause.
Consultation
In establishing the procedures under paragraph (1), the Secretary shall consult with the Inspector General of the Department of Health and Human Services, affected industry, consumers, consumer advocates, and other interested parties in order to ensure that the information made available to the public under such paragraph is presented in the appropriate overall context.
Annual reports and relation to State laws
Annual report to Congress
Annual reports to States
Not later than and on June 30 of each calendar year thereafter, the Secretary shall submit to States a report that includes a summary of the information submitted under subsection (a) during the preceding year with respect to covered recipients in the State (except, in the case of information submitted with respect to a payment or other transfer of value described in subsection (c)(1)(E)(i), such information shall be included in the first report submitted to States after the date on which such information is made available to the public under such subsection).
Relation to State laws
In general .—
No preemption of additional requirements .—
Consultation
The Secretary shall consult with the Inspector General of the Department of Health and Human Services on the implementation of this section.
Definitions
Applicable group purchasing organization
The term “applicable group purchasing organization” means a group purchasing organization (as defined by the Secretary) that purchases, arranges for, or negotiates the purchase of a covered drug, device, biological, or medical supply which is operating in the United States, or in a territory, possession, or commonwealth of the United States.
Applicable manufacturer
The term “applicable manufacturer” means a manufacturer of a covered drug, device, biological, or medical supply which is operating in the United States, or in a territory, possession, or commonwealth of the United States.
Clinical investigation
The term “clinical investigation” means any experiment involving 1 or more human subjects, or materials derived from human subjects, in which a drug or device is administered, dispensed, or used.
Covered device
The term “covered device” means any device for which payment is available under subchapter XVIII or a State plan under subchapter XIX or XXI (or a waiver of such a plan).
Covered drug, device, biological, or medical supply
The term “covered drug, device, biological, or medical supply” means any drug, biological product, device, or medical supply for which payment is available under subchapter XVIII or a State plan under subchapter XIX or XXI (or a waiver of such a plan).
Covered recipient
In general
Exclusion
Such term does not include a physician, physician assistant, nurse practitioner, clinical nurse specialist, certified nurse anesthetist, or certified nurse-midwife who is an employee of the applicable manufacturer that is required to submit information under subsection (a).
Employee
section 1395nn(h)(2) of this titleThe term “employee” has the meaning given such term in .
Knowingly
section 3729(b) of title 31The term “knowingly” has the meaning given such term in .
Manufacturer of a covered drug, device, biological, or medical supply
The term “manufacturer of a covered drug, device, biological, or medical supply” means any entity which is engaged in the production, preparation, propagation, compounding, or conversion of a covered drug, device, biological, or medical supply (or any entity under common ownership with such entity which provides assistance or support to such entity with respect to the production, preparation, propagation, compounding, conversion, marketing, promotion, sale, or distribution of a covered drug, device, biological, or medical supply).
Payment or other transfer of value
In general
The term “payment or other transfer of value” means a transfer of anything of value. Such term does not include a transfer of anything of value that is made indirectly to a covered recipient through a third party in connection with an activity or service in the case where the applicable manufacturer is unaware of the identity of the covered recipient.
Exclusions
Physician
section 1395x(r) of this titleThe term “physician” has the meaning given that term in .
Aug. 14, 1935, ch. 531Pub. L. 111–148, title VI, § 6002124 Stat. 689Pub. L. 115–271, title VI, § 6111(a)(1)132 Stat. 4006(, title XI, § 1128G, as added , , ; amended , (b), , , 4007.)
Editorial Notes
Amendments
Pub. L. 115–271, § 6111(b)2018—Subsec. (c)(1)(C)(viii). , substituted “in the case of information made available under this subparagraph prior to , does not contain” for “does not contain”.
Pub. L. 115–271, § 6111(a)(1)(A)Subsec. (e)(6)(A)(iii) to (v). , added cls. (iii) to (v).
Pub. L. 115–271, § 6111(a)(1)(B)Subsec. (e)(6)(B). , inserted “, physician assistant, nurse practitioner, clinical nurse specialist, certified nurse anesthetist, or certified nurse-midwife” after “physician”.
Statutory Notes and Related Subsidiaries
Effective Date of 2018 Amendment
Pub. L. 115–271, title VI, § 6111(a)(2)132 Stat. 4006
Administration
Pub. L. 115–271, title VI, § 6111(c)132 Stat. 4007