cfr_sections
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
15 rows where part_number = 159 and title_number = 40 sorted by section_id
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| section_id ▼ | title_number | title_name | chapter | subchapter | part_number | part_name | subpart | subpart_name | section_number | section_heading | agency | authority | source_citation | amendment_citations | full_text |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 40:40:26.0.1.1.10.2.1.1 | 40 | Protection of Environment | I | E | 159 | PART 159—STATEMENTS OF POLICIES AND INTERPRETATIONS | D | Subpart D—Reporting Requirements for Risk/Benefit Information | § 159.152 What the law requires of registrants. | EPA | (a) Section 6(a)(2) of the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA) states: “If at any time after the registration of a pesticide the registrant has additional factual information regarding unreasonable adverse effects on the environment of the pesticide, he shall submit such information to the Administrator.” (b) Section 152.50(f)(3) of this chapter requires applicants to submit, as part of an application for registration, any factual information of which he is aware regarding unreasonable adverse effects of the pesticide on humans or the environment, which would be required to be reported under section 6(a)(2) if the product were registered. (c) Compliance with this part will satisfy a registrant's obligations to submit additional information pursuant to section 6(a)(2) and will satisfy an applicant's obligation to submit additional information pursuant to § 152.50(f)(3) of this chapter. | ||||
| 40:40:26.0.1.1.10.2.1.10 | 40 | Protection of Environment | I | E | 159 | PART 159—STATEMENTS OF POLICIES AND INTERPRETATIONS | D | Subpart D—Reporting Requirements for Risk/Benefit Information | § 159.170 Human epidemiological and exposure studies. | EPA | Information must be submitted which concerns any study that a person described in § 159.158(a) has concluded, or might reasonably conclude, shows that a correlation may exist between exposure to a pesticide and observed adverse effects in humans. Information must also be submitted which concerns exposure monitoring studies that indicate higher levels of risk or exposure than would be expected based on previously available reports, data, or exposure estimates. Such information must be submitted regardless of whether the registrant considers any observed correlation or association to be significant. | ||||
| 40:40:26.0.1.1.10.2.1.11 | 40 | Protection of Environment | I | E | 159 | PART 159—STATEMENTS OF POLICIES AND INTERPRETATIONS | D | Subpart D—Reporting Requirements for Risk/Benefit Information | § 159.178 Information on pesticides in or on food, feed or water. | EPA | [62 FR 49388, Sept. 19, 1997; 63 FR 33582, June 19, 1998] | (a) Food and feed. Information must be submitted if it shows that the pesticide is present in or on food or feed at a level in excess of established levels, except that information on excess residues resulting solely from studies conducted under authority of FIFRA section 5 or under other controlled research studies conducted to test a pesticide product need not be submitted, provided that the treated crop is not marketed as a food or feed commodity. The information to be submitted is the same as that required in § 159.184(c)(1), (2), (3), and (4)(iv)(E), (F), (G), and (H). (b) Water. (1) Information must be submitted if it shows that a pesticide is present above the water reference level in any of the following instances: (i) Waters of the United States, as defined in § 122.2 of this chapter, except paragraph (d) of § 122.2. (ii) Ground water. (iii) Finished drinking water. (2) If the lowest detectable amount of the pesticide is reported, the detection limit must also be reported. (3) Information need not be submitted regarding the detection of a pesticide in waters of the United States or finished drinking water if the pesticide is registered for use in finished drinking water or surface water and the amount detected does not exceed the amounts reported by a registrant in its application for registration, as resulting in those waters from legal applications of the pesticide. (4) Information need not be submitted concerning detections of pesticides in waters of the United States, ground water or finished drinking water if the substance detected is an inert ingredient, or a metabolite, degradate, contaminant or impurity of a pesticide product, unless EPA has established or proposed a maximum contaminant level (MCL) or health advisory level (HAL) for that substance, or has estimated a health advisory level based on an established reference dose (RfD) for that substance, and notified registrants of that level. (5) Information to be submitted is the same as that required in § 159.184(c)(1), (2), (3), (4)… | |||
| 40:40:26.0.1.1.10.2.1.12 | 40 | Protection of Environment | I | E | 159 | PART 159—STATEMENTS OF POLICIES AND INTERPRETATIONS | D | Subpart D—Reporting Requirements for Risk/Benefit Information | § 159.179 Metabolites, degradates, contaminants, and impurities. | EPA | [62 FR 49388, Sept. 19, 1997; 63 FR 33582, June 19, 1998] | (a) Metabolites and degradates. Information which shows the existence of any metabolite or degradate of a pesticide product must be submitted if either of the following conditions is met: (1) The metabolite or degradate may occur or be present under conditions of use of the pesticide product, and the existence of the metabolite or degradate or the association of the metabolite or degradate with the pesticide product has not been previously reported to EPA. (2) The metabolite or degradate has been previously reported, but it is detected at levels higher than any previously reported; and either of the following conditions is met: (i) Any person described in § 159.158(a) has concluded that the metabolite or degradate may pose a toxicological or ecological risk based on any one or more of the following: (A) The physical or chemical properties of the metabolite or degradate. (B) Data regarding structurally analogous chemicals. (C) Data regarding chemical reactivity of the metabolite or degradate and structurally analogous substances. (D) Data on the metabolite or degradate. (ii) The registrant has concluded, or has been advised by any person described in § 159.158(a) that the metabolite or degradate, or analogous chemicals, may have any experimentally determined half-life greater than 3 weeks as shown from laboratory aerobic soil metabolism studies or field dissipation studies, or may have any experimentally determined resistance to hydrolytic degradation, or photolytic degradation on soil or in water, under any conditions, resulting in degradation of less than 10 percent in a 30-day period. (b) Contaminants and impurities. The presence in any pesticide product of a contaminant or impurity not previously identified by the registrant as part of the pesticide product's approved composition must be reported pursuant to this part if the contaminant or impurity is present in the product in any of the following quantities: (1) Quantities greater than 0.1 percent by weight (1,000 parts per million). (2) Quanti… | |||
| 40:40:26.0.1.1.10.2.1.13 | 40 | Protection of Environment | I | E | 159 | PART 159—STATEMENTS OF POLICIES AND INTERPRETATIONS | D | Subpart D—Reporting Requirements for Risk/Benefit Information | § 159.184 Toxic or adverse effect incident reports. | EPA | [62 FR 49388, Sept. 19, 1997; 63 FR 33583, June 19, 1998] | (a) General. Information about incidents affecting humans or other non-target organisms must be submitted if the following three conditions are met: (1) The registrant is aware, or has been informed that a person or non-target organism may have been exposed to a pesticide. (2) The registrant is aware, or has been informed that the person or non-target organism suffered a toxic or adverse effect, or may suffer a delayed or chronic adverse effect in the future. (3) The registrant has or could obtain information concerning where the incident occurred, the pesticide or product involved, and the name of a person to contact regarding the incident. (b) Exceptions. Information regarding an incident need not be submitted if any of the following conditions are met: (1) The registrant is aware of facts which clearly establish that the reported toxic effect, or reported exposure, did not or will not occur. (2) The registrant has been notified in writing by the Agency that the reporting requirement has been waived for this incident or category of incidents, and the registrant has not been notified in writing by the Agency that the waiver is rescinded. (3) It concerns a toxic effect to non-target plants, which were at the use site at the time the pesticide was applied, if the label provides adequate notice of such a risk. (4) It concerns non-lethal phytotoxicity to the treated crop if the label provides an adequate notice of such a risk. (5) It concerns a toxic effect to pests not specified on the label, provided that such pests are similar to pests specified on the label. (6) It concerns minor skin or eye irritation effects warned of on the label of a product which is registered for use in residential use sites, and the effects occurred as a result of use in a residential site. (c) Required information on individual incidents. To the extent that the registrant has any of the information listed in paragraphs (c)(1) through (c)(4) of this section, the registrant must supply the information on each pesticide inc… | |||
| 40:40:26.0.1.1.10.2.1.14 | 40 | Protection of Environment | I | E | 159 | PART 159—STATEMENTS OF POLICIES AND INTERPRETATIONS | D | Subpart D—Reporting Requirements for Risk/Benefit Information | § 159.188 Failure of performance information. | EPA | [63 FR 49388, Sept. 19, 1997, as amended at 72 FR 61029, Oct. 26, 2007] | (a) Microorganisms that pose a risk to human health. Information must be submitted which concerns either incidents described in paragraph (a)(1) of this section or a study described in paragraph (a)(2) of this section: (1) Information which concerns an incident which meets all of the following conditions: (i) The registrant has been informed that a pesticide product may not have performed as claimed against target microorganisms. (ii) The possible failures of the pesticide to perform as claimed involved the use against microorganisms which may pose a risk to human health. (iii) The pesticide product's use site is other than residential. (iv) The registrant has or could obtain information concerning where the incident occurred, the pesticide or product involved, and the name of a person to contact regarding the incident. (2) A study which indicates that the pesticide may not perform in accordance with one or more claims made by the registrant regarding uses intended for control of microorganisms tha may pose a risk to human health, including any of the public health antimicrobials identified in part 161 of this chapter. (b) Animals that pose a risk to human health. For the purposes of this section, any animal (including insects) poses a risk to human health if it may cause disease in humans, either directly or as a disease vector; produce toxins that are harmful to humans; or cause direct physical harm to humans. Information must be submitted which concerns either incidents described in paragraph (b)(1) of this section or a study described in paragraph (b)(2) of this section. (1) Information which concerns an incident which meets all of the following conditions: (i) The registrant has been informed by municipal, State, or Federal public health officials that a pesticide product may not have performed as claimed against target animals. (ii) The possible failures of the pesticide to perform as claimed involved the use against animals that pose a risk to human health. (iii) The registrant has or could … | |||
| 40:40:26.0.1.1.10.2.1.15 | 40 | Protection of Environment | I | E | 159 | PART 159—STATEMENTS OF POLICIES AND INTERPRETATIONS | D | Subpart D—Reporting Requirements for Risk/Benefit Information | § 159.195 Reporting of other information. | EPA | [62 FR 49388, Sept. 19, 1997; 63 FR 33583, June 19, 1998] | (a) The registrant shall submit to the Administrator information other than that described in §§ 159.165 through 159.188 if the registrant knows, or reasonably should know, that if the information should prove to be correct, EPA might regard the information alone or in conjunction with other information about the pesticide as raising concerns about the continued registration of a product or about the appropriate terms and conditions of registration of a product. Examples of the types of information which must be provided if not already reportable under some other provision of this part include but are not limited to information showing: (1) Previously unknown or unexpected bioaccumulation of a pesticide by various life forms. (2) Greater than anticipated drift of pesticides to non-target areas. (3) Use of a pesticide may pose any greater risk than previously believed or reported to the Agency. (4) Use of a pesticide promotes or creates secondary pest infestations. (5) Any information which might tend to invalidate a study submitted to the Agency to support a pesticide registration. (b) A registrant is not obligated under paragraph (a) of this section to provide information to the Administrator if the registrant is aware of facts which establish that otherwise reportable information is not correct. (c) The registrant shall submit to the Administrator information other than that described in §§ 159.165 through 159.188 if the registrant has been informed by EPA that such additional information has the potential to raise questions about the continued registration of a product or about the appropriate terms and conditions of registration of a product. | |||
| 40:40:26.0.1.1.10.2.1.2 | 40 | Protection of Environment | I | E | 159 | PART 159—STATEMENTS OF POLICIES AND INTERPRETATIONS | D | Subpart D—Reporting Requirements for Risk/Benefit Information | § 159.153 Definitions. | EPA | [62 FR 49388, Sept. 19, 1997, as amended at 63 FR 33582, June 19, 1998; 73 FR 75596, Dec. 12, 2008] | (a) For the purposes of reporting information pursuant to FIFRA section 6(a)(2), the definitions set forth in FIFRA section 2 and in 40 CFR part 152 apply to this part unless superseded by a definition in paragraph (b) of this section. (b) For purposes of reporting information pursuant to FIFRA section 6(a)(2), the following definitions apply only to this subpart: Established level means a tolerance, temporary tolerance, food additive regulation, action level, or other limitation on pesticide residues imposed by law, regulation, or other authority. Formal Review means Special Review, Rebuttable Presumption Against Registration (RPAR), FIFRA section 6(c) suspension proceeding, or FIFRA section 6(b) cancellation proceeding, whether completed or not. Hospitalization means admission for treatment to a hospital, clinic or other health care facility. Treatment as an out-patient is not considered to be hospitalization. Maximum contaminant level (MCL) means the maximum permissible level, established by EPA, for a contaminant in water which is delivered to any user of a public water system. Non-target organism means any organism for which pesticidal control was either not intended or not legally permitted by application of a pesticide. Pesticide means a pesticide product which is or was registered by EPA, and each active ingredient, inert ingredient, impurity, metabolite, contaminant or degradate contained in, or derived from, such pesticide product. Qualified expert means one who, by virtue of his or her knowledge, skill, experience, training, or education, could be qualified by a court as an expert to testify on issues related to the subject matter on which he or she renders a conclusion or opinion. Under Rule 702 of the Federal Rules of Evidence, a person may be qualified as an expert on a particular matter by virtue of “knowledge, skill, experience, training, or education.” In general, EPA wants registrants to report information when a person has relevant expert credentials, e.g., a medical doctor givin… | |||
| 40:40:26.0.1.1.10.2.1.3 | 40 | Protection of Environment | I | E | 159 | PART 159—STATEMENTS OF POLICIES AND INTERPRETATIONS | D | Subpart D—Reporting Requirements for Risk/Benefit Information | § 159.155 When information must be submitted. | EPA | [63 FR 33582, June 19, 1998] | (a) The following reportable information must be received by EPA not later than the 30th calendar day after the registrant first possesses or knows of the information: (1) Scientific studies described in § 159.165. (2) Information about discontinued studies described in § 159.167. (3) Human epidemiological and exposure studies described in § 159.170. (4) Detection of a pesticide in or on food or feed described in § 159.178(a). (5) Detection of metabolites, degradates, contaminates, impurities described in § 159.179. (6) Failure of performance studies described in § 159.188(a)(2), (b)(2), and (c). (7) Other information described in § 159.195. (b) Reportable information concerning detections of pesticides in water described in § 159.178(b), adverse effects incidents described in § 159.184(a), and efficacy failure incidents described in § 159.188(a)(1) and (b)(1) must be reported according to the time frames set forth in § 159.184(d). (c) EPA may, in its discretion, notify a registrant in writing of a different reporting period that will apply to specific types of reportable information or eliminate reporting requirements entirely. Such notification supersedes otherwise applicable reporting requirements set forth in this part. (d) For purposes of this part, a registrant possesses or knows of information at the time any officer, employee, agent, or other person acting for the registrant first comes into possession of, or knows of, such information; provided that, such person performs any activities for the registrant related to the development, testing, sale or registration of a pesticide or the person could be reasonably expected to come into possession of information otherwise reportable under this part. In the case of information known to or possessed by an agent or other person acting for the registrant, a registrant is responsible for such information only if the agent or other person acquired such information while acting for the registrant. | |||
| 40:40:26.0.1.1.10.2.1.4 | 40 | Protection of Environment | I | E | 159 | PART 159—STATEMENTS OF POLICIES AND INTERPRETATIONS | D | Subpart D—Reporting Requirements for Risk/Benefit Information | § 159.156 How information must be submitted. | EPA | [63 FR 49388, Sept. 19, 1997, as amended at 69 FR 39864, July 1, 2004; 71 FR 35545, June 21, 2006; 72 FR 61028, Oct. 26, 2007] | A submission under FIFRA section 6(a)(2) must be delivered to the Office of Pesticide Programs' Document Processing Desk at the appropriate address as set forth in 40 CFR 150.17(a) or (b). (a) Include a cover letter which contains the information requested in paragraphs (d) and (e) of this section, and a prominent statement that the information is being submitted in accordance with FIFRA section 6(a)(2). (b) Contain the name of the submitter, registrant name and registration number, date of transmittal to EPA, the type of study or incident being reported under §§ 159.165 through 159.195, and a statement of why the information is considered reportable under this part. (c) Identify the substance tested or otherwise covered by the information (including, if known, the EPA registration number(s) to which the information pertains, and if known, the CAS Registry Number). (d) In reporting incidents, provide the data listed in § 159.184, to the extent such information is available. (e) In submitting scientific studies, follow the procedures set forth in § 158.32 or § 161.32 of this chapter, as applicable. (f) If the information is part of a larger package being submitted in order to comply with another provision of FIFRA (e.g., sections 3(c)(2)(B), 4(e)(1)(E)), identify in the transmittal the individual studies being submitted under this part. (g) If a claim of confidentiality is made under FIFRA section 10 for information relating to any part of a study or incident report contained in the submission, follow the procedures set forth in § 158.33 or § 161.33 of this chapter, as applicable regarding the identification and segregation of information claimed to be confidential. (h) If a submission includes a study subject to the flagging requirements of § 158.34 or § 161.34 of this chapter, as applicable, comply with the requirements of that section, and, if the flagging statement is positive, identify it as 6(a)(2) information in the transmittal. (i) If a submission is a follow-up to an earlier study or incident rep… | |||
| 40:40:26.0.1.1.10.2.1.5 | 40 | Protection of Environment | I | E | 159 | PART 159—STATEMENTS OF POLICIES AND INTERPRETATIONS | D | Subpart D—Reporting Requirements for Risk/Benefit Information | § 159.158 What information must be submitted. | EPA | [62 FR 49388, Sept. 19, 1997; 63 FR 33582, June 19, 1998] | (a) General. Information which is reportable under this part must be submitted if the registrant possesses or receives the information, and the information is relevant to the assessment of the risks or benefits of one or more specific pesticide registrations currently or formerly held by the registrant. Information relevant to the assessment of the risks or benefits also includes conclusion(s) or opinion(s) rendered by a person who meets any of the following: (1) Who was employed or retained (directly or indirectly) by the registrant, and was likely to receive such information. (2) From whom the registrant requested the opinion(s) or conclusion(s) in question. (3) Who is a qualified expert as described in § 159.153(b). (b) Exceptions —(1) Clearly erroneous information. Information need not be submitted if before that date on which the registrant must submit such information if all of the following conditions are met: (i) The registrant discovers that any analysis, conclusion, or opinion was predicated on data that were erroneously generated, recorded, or transmitted, or on computational errors. (ii) Every author of each such analysis, conclusion, or opinion, or as many authors as can be contacted through the use of reasonable diligence, has acknowledged in writing that the analysis, conclusion, or opinion was improper and has either corrected the original analysis, conclusion, or opinion accordingly, or provided an explanation as to why it cannot be corrected. (iii) As a result of the correction, the information is no longer required to be reported under FIFRA section 6(a)(2), or if no correction was possible, the authors agree that the original analysis, conclusion or opinion has no scientific validity. (2) Previously submitted information. Information regarding an incident, study, or other occurrence need not be submitted if before the date on which the registrant must submit such information, the registrant is aware that the reportable information concerning that incident, study, or other occurr… | |||
| 40:40:26.0.1.1.10.2.1.6 | 40 | Protection of Environment | I | E | 159 | PART 159—STATEMENTS OF POLICIES AND INTERPRETATIONS | D | Subpart D—Reporting Requirements for Risk/Benefit Information | § 159.159 Information obtained before promulgation of the rule. | EPA | [62 FR 49388, Sept. 19, 1997; 63 FR 33582, June 19, 1998, as amended at 63 FR 41193, Aug. 3, 1998] | (a) Notwithstanding any other provision of this part, information held by registrants on August 17, 1998 which has not been previously submitted to the Agency, but which is reportable under the terms of this part, must be submitted to the Agency if it meets any of the following criteria: (1) Information is otherwise reportable under § 159.184, and pertains to an incident that is alleged to have occurred on or after January 1, 1994, and to have involved any of the following: (i) A fatality or hospitalization of a human being. (ii) A fatality of a domestic animal. (iii) A fatality or fatalities to fish or wildlife, if the incident meets the criteria for the exposure type and severity category designation “W-A” set forth in § 159.184(c)(5)(iii). (2) Submission of the information is requested by the Agency pursuant to § 159.195(c). (b) If a registrant possesses information required to be submitted by paragraph (a)(1) of this section, the registrant must submit on or before June 16, 1999 in accordance with § 159.156(c), (d), and (e) an inventory of the incidents that meet the requirements of paragraphs (a)(1) of this section. Such an inventory must include the separate number of incidents that meet the requirements of paragraphs (a)(1)(i), (a)(1)(ii), and (a)(1)(iii) of this section, and for each type of incident, the total numbers of fatalities or hospitalizations involved. (c) If a registrant possesses information required to be submitted by paragraph (a)(2) of this section, the information must be submitted in accordance with any schedule contained in the Agency's request for the information. | |||
| 40:40:26.0.1.1.10.2.1.7 | 40 | Protection of Environment | I | E | 159 | PART 159—STATEMENTS OF POLICIES AND INTERPRETATIONS | D | Subpart D—Reporting Requirements for Risk/Benefit Information | § 159.160 Obligations of former registrants. | EPA | [62 FR 49388, Sept. 19, 1997; 63 FR 33582, June 19, 1998, as amended at 73 FR 75596, Dec. 12, 2008] | (a) General. A former registrant is obliged to continue to submit information concerning the registration of a pesticide product previously held by the registrant and otherwise reportable under the provisions of this part for a period of 5 years after the registration of the pesticide product has been canceled or transferred to another registrant, with the exceptions provided by paragraph (b) of this section. (b) Exceptions. Notwithstanding the provisions of paragraph (a) of this section, a former registrant is not obligated to report information pursuant to this part if any of the following conditions are applicable: (1) The information is first obtained by the person more than 1 year after the date on which the person ceased to hold the registration of the product to which the information pertains, and the person holds no active pesticide registrations, or for some other reason cannot reasonably be expected to receive information concerning the formerly registered product. (2) The information is associated solely with an inert ingredient, contaminant, impurity, metabolite, or degradate contained in a product, and the information is first obtained by the person more than 1 year after the date upon which the person ceased to hold the registration of the product. (3) The information is associated with an active ingredient or a formerly registered product, and the active ingredient or every active ingredient contained in the formerly registered product has not been contained in any pesticide product registered in the United States for any part of the 3-year period preceding the date on which the person first obtained the information. (4) The information pertains solely to a formerly registered product that no longer meets the definition of “pesticide” in section 2(u) of FIFRA. (c) Information arising from litigation. Notwithstanding any other provisions of this section, a former registrant is obliged to submit information otherwise reportable under this part concerning formerly-registered pesticide prod… | |||
| 40:40:26.0.1.1.10.2.1.8 | 40 | Protection of Environment | I | E | 159 | PART 159—STATEMENTS OF POLICIES AND INTERPRETATIONS | D | Subpart D—Reporting Requirements for Risk/Benefit Information | § 159.165 Toxicological and ecological studies. | EPA | [62 FR 49388, Sept. 19, 1997; 63 FR 33582, June 19, 1998; 73 FR 75597, Dec. 12, 2008] | Adverse effects information must be submitted as follows: (a) Toxicological studies. (1) The results of a study of the toxicity of a pesticide to humans or other non-target domestic organisms if, relative to all previously submitted studies, they show an adverse effect under any of the following conditions: (i) That is in a different organ or tissue of the test organism. (ii) At a lower dosage, or after a shorter exposure period, or after a shorter latency period. (iii) At a higher incidence or frequency. (iv) In a different species, strain, sex, or generation of test organism. (v) By a different route of exposure. (2) Acute oral, acute dermal, acute inhalation or skin and eye irritation studies in which the only change in toxicity is a numerical decrease in the median lethal dose (LD 50 ), median lethal concentration (LC 50 ) or irritation indices, are not reportable under this part unless the results indicate a more restrictive toxicity category for labeling under the criteria of 40 CFR 156.62. (b) Ecological studies. The results of a study of the toxicity of a pesticide to terrestrial or aquatic wildlife or plants if, relative to all previously submitted studies, they show an adverse effect under any of the following conditions: (1) At levels 50 percent or more lower than previous acute toxicity studies with similar species, including determinations of the median lethal dose (LD 50 ), median lethal concentration (LC 50 ), or median effective concentration (EC 50 ). (2) At lower levels in a chronic study than previous studies with similar species. (3) In a study with a previously untested species the results indicate the chronic no observed effect level (NOEL) is 10 percent or less of the lowest LC 50 or LD 50 for a similar species. (4) For plants when tested at the maximum label application rate or less, if either of the following conditions is met: (i) More than 25 percent of terrestrial plants show adverse effects on plant life cycle functions and growth such as germination, emergence, pla… | |||
| 40:40:26.0.1.1.10.2.1.9 | 40 | Protection of Environment | I | E | 159 | PART 159—STATEMENTS OF POLICIES AND INTERPRETATIONS | D | Subpart D—Reporting Requirements for Risk/Benefit Information | § 159.167 Discontinued studies. | EPA | The fact that a study has been discontinued before the planned termination must be reported to EPA, with the reason for termination, if submission of information concerning the study is, or would have been, required under this part. |
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CREATE TABLE cfr_sections (
section_id TEXT PRIMARY KEY,
title_number INTEGER,
title_name TEXT,
chapter TEXT,
subchapter TEXT,
part_number TEXT,
part_name TEXT,
subpart TEXT,
subpart_name TEXT,
section_number TEXT,
section_heading TEXT,
agency TEXT,
authority TEXT,
source_citation TEXT,
amendment_citations TEXT,
full_text TEXT
);
CREATE INDEX idx_cfr_title ON cfr_sections(title_number);
CREATE INDEX idx_cfr_part ON cfr_sections(part_number);
CREATE INDEX idx_cfr_agency ON cfr_sections(agency);