Sec. 1001. DISCONTINUANCE OR INTERRUPTION IN THE PRODUCTION OF LIFE-SAVING DRUGS
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## SEC. 1001 DISCONTINUANCE OR INTERRUPTION IN THE PRODUCTION OF LIFE-SAVING DRUGS ###
(a)In General Section 506C (21 U.S.C. 356c) is amended to read as follows: > > ## “SEC. 506C DISCONTINUANCE OR INTERRUPTION IN THE PRODUCTION OF LIFE-SAVING DRUGS > > > ### “(a) In General > > A manufacturer of a drug— > > > #### “(1) > > that is— > > > ##### “(A) > > life-supporting; > > > ##### “(B) > > life-sustaining; or > > > ##### “(C) > > intended for use in the prevention or treatment of a debilitating disease or condition, including any such drug used in emergency medical care or during surgery; and > > > #### “(2) > > that is not a radio pharmaceutical drug product or any other product as designated by the Secretary, > > shall notify the Secretary, in accordance with subsection (b), of a permanent discontinuance in the manufacture of the drug or an interruption of the manufacture of the drug that is likely to lead to a meaningful disruption in the supply of that drug in the United States, and the reasons for such discontinuance or interruption. > > > ### “(b) Timing > > A notice required under subsection
(a)shall be submitted to the Secretary— > > > #### “(1) > > at least 6 months prior to the date of the discontinuance or interruption; or > > > #### “(2) > > if compliance with paragraph
(1)is not possible, as soon as practicable. > > > ### “(c) Distribution > > To the maximum extent practicable, the Secretary shall distribute, through such means as the Secretary deems appropriate, information on the discontinuation or interruption of the manufacture of the drugs described in subsection
(a)to appropriate organizations, including physician, health provider, and patient organizations, as described in section 506E. > > > ### “(d) Confidentiality > > Nothing in this section shall be construed as authorizing the Secretary to disclose any information that is a trade secret or confidential information subject to section 552(b)(4) of title 5, United States Code, or section 1905 of title 18, United States Code. > > > ### “(e) Coordination With Attorney General > > Not later than 30 days after the receipt of a notification described in subsection (a), the Secretary shall— > > > #### “(1) > > determine whether the notification pertains to a controlled substance subject to a production quota under section 306 of the Controlled Substances Act; and > > > #### “(2) > > if necessary, as determined by the Secretary— > > > ##### “(A) > > notify the Attorney General that the Secretary has received such a notification; > > > ##### “(B) > > request that the Attorney General increase the aggregate and individual production quotas under section 306 of the Controlled Substances Act applicable to such controlled substance and any ingredient therein to a level the Secretary deems necessary to address a shortage of a controlled substance based on the best available market data; and > > > ##### “(C) > > if the Attorney General determines that the level requested is not necessary to address a shortage of a controlled substance, the Attorney General shall provide to the Secretary a written response detailing the basis for the Attorney General’s determination. > > The Secretary shall make the written response provided under subparagraph
(C)available to the public on the Internet Web site of the Food and Drug Administration. > > > ### “(f) Failure To Meet Requirements > > If a person fails to submit information required under subsection
(a)in accordance with subsection (b)— > > > #### “(1) > > the Secretary shall issue a letter to such person informing such person of such failure; > > > #### “(2) > > not later than 30 calendar days after the issuance of a letter under paragraph (1), the person who receives such letter shall submit to the Secretary a written response to such letter setting forth the basis for noncompliance and providing information required under subsection (a); and > > > #### “(3) > > not later than 45 calendar days after the issuance of a letter under paragraph (1), the Secretary shall make such letter and any response to such letter under paragraph
(2)available to the public on the Internet Web site of the Food and Drug Administration, with appropriate redactions made to protect information described in subsection (d), except that, if the Secretary determines that the letter under paragraph
(1)was issued in error or, after review of such response, the person had a reasonable basis for not notifying as required under subsection (a), the requirements of this paragraph shall not apply. > > > ### “(g) Expedited Inspections and Reviews > > If, based on notifications described in subsection
(a)or any other relevant information, the Secretary concludes that there is, or is likely to be, a drug shortage of a drug described in subsection (a), the Secretary may— > > > #### “(1) > > expedite the review of a supplement to a new drug application submitted under section 505(b), an abbreviated new drug application submitted under section 505(j), or a supplement to such an application submitted under section 505(j) that could help mitigate or prevent such shortage; or > > > #### “(2) > > expedite an inspection or reinspection of an establishment that could help mitigate or prevent such drug shortage. > > > ### “(h) Definitions > > For purposes of this section— > > > #### “(1) > > the term ‘drug’— > > > ##### “(A) > > means a drug (as defined in section 201(g)) that is intended for human use and that is subject to section 503(b)(1); and > > > ##### “(B) > > does not include biological products (as defined in section 351 of the Public Health Service Act), unless otherwise provided by the Secretary in the regulations promulgated under subsection (i); > > > #### “(2) > > the term ‘drug shortage’ or ‘shortage’, with respect to a drug, means a period of time when the demand or projected demand for the drug within the United States exceeds the supply of the drug; and > > > #### “(3) > > the term ‘meaningful disruption’— > > > ##### “(A) > > means a change in production that is reasonably likely to lead to a reduction in the supply of a drug by a manufacturer that is more than negligible and affects the ability of the manufacturer to fill orders or meet expected demand for its product; and > > > ##### “(B) > > does not include interruptions in manufacturing due to matters such as routine maintenance or insignificant changes in manufacturing so long as the manufacturer expects to resume operations in a short period of time. > > > ### “(i) Regulations > > > #### “(1) In general > > Not later than 18 months after the date of enactment of the Food and Drug Administration Safety and Innovation Act, the Secretary shall adopt a final regulation implementing this section. > > > #### “(2) Contents > > Such regulation shall define, for purposes of this section, the terms ‘life-supporting’, ‘life-sustaining’, and ‘intended for use in the prevention or treatment of a debilitating disease or condition’. > > > #### “(3) Inclusion of biological products > > > ##### “(A) In general > > The Secretary may by regulation apply this section to biological products (as defined in section 351 of the Public Health Service Act), including plasma products derived from human plasma protein and their recombinant analogs, if the Secretary determines such inclusion would benefit the public health. Such regulation shall take into account any supply reporting programs and shall aim to reduce duplicative notification. > > > ##### “(B) Rule for vaccines > > If the Secretary applies this section to vaccines pursuant to subparagraph (A), the Secretary shall— > > > ###### “(i) > > consider whether the notification requirement under subsection
(a)may be satisfied by submitting a notification to the Centers for Disease Control and Prevention under the vaccine shortage notification program of such Centers; and > > > ###### “(ii) > > explain the determination made by the Secretary under clause
(i)in the regulation. > > > #### “(4) Procedure > > In promulgating a regulation implementing this section, the Secretary shall— > > > ##### “(A) > > issue a notice of proposed rulemaking that includes the proposed regulation; > > > ##### “(B) > > provide a period of not less than 60 days for comments on the proposed regulation; and > > > ##### “(C) > > publish the final regulation not less than 30 days before the regulation’s effective date. > > > #### “(5) Restrictions > > Notwithstanding any other provision of Federal law, in implementing this section, the Secretary shall only promulgate regulations as described in paragraph (4).” > . ###
(b)Effect of Notification **[**[21 U.S.C. 356c note](/us/usc/t21/s356c)**]** The submission of a notification to the Secretary of Health and Human Services (referred to in this title as the “Secretary”) for purposes of complying with the requirement in section 506C(a) of the Federal Food, Drug, and Cosmetic Act (as amended by subsection (a)) shall not be construed— ####
(1)as an admission that any product that is the subject of such notification violates any provision of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 301 et seq.); or ####
(2)as evidence of an intention to promote or market the product for an indication or use for which the product has not been approved by the Secretary.
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Sec. 1001
DISCONTINUANCE OR INTERRUPTION IN THE PRODUCTION OF LIFE-SAVING DRUGS
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