Information Collection Request Submitted to OMB for Review and Approval; Comment Request; Laboratory Quality Assurance Evaluation Program for Analysis of Cryptosporidium Under the Safe Drinking Water Act (Renewal), 4478-4479 [2018-01899]

Download as PDF sradovich on DSK3GMQ082PROD with NOTICES 4478 Federal Register / Vol. 83, No. 21 / Wednesday, January 31, 2018 / Notices Docket Numbers: ER16–1901–005. Applicants: Elevation Solar C LLC. Description: Compliance filing: Elevation Solar C LLC Notice of Change in Status to be effective 1/26/2018. Filed Date: 1/25/18. Accession Number: 20180125–5099. Comments Due: 5 p.m. ET 2/15/18. Docket Numbers: ER16–1973–005. Applicants: Western Antelope Blue Sky Ranch B LLC. Description: Compliance filing: Western Antelope Blue Sky Ranch B Change in Status to be effective 1/26/2018. Filed Date: 1/25/18. Accession Number: 20180125–5115. Comments Due: 5 p.m. ET 2/15/18. Docket Numbers: ER16–2578–005. Applicants: North Lancaster Ranch LLC. Description: Compliance filing: North Lancaster Ranch Change in Status to be effective 1/26/2018. Filed Date: 1/25/18. Accession Number: 20180125–5110. Comments Due: 5 p.m. ET 2/15/18. Docket Numbers: ER18–713–000. Applicants: CA Flats Solar 150, LLC. Description: Baseline eTariff Filing: CA Flats Solar 150, LLC MBR Tariff to be effective 3/26/2018. Filed Date: 1/25/18. Accession Number: 20180125–5026. Comments Due: 5 p.m. ET 2/15/18. Docket Numbers: ER18–714–000. Applicants: Southern California Edison Company. Description: § 205(d) Rate Filing: Luz Solar Partners LTD., V LGIA Kramer Junction 5 Project SA No. 207, TOT694 to be effective 2/2/2018. Filed Date: 1/25/18. Accession Number: 20180125–5046. Comments Due: 5 p.m. ET 2/15/18. Docket Numbers: ER18–715–000. Applicants: PJM Interconnection, L.L.C. Description: § 205(d) Rate Filing: Original WMPA SA No. 4905; Queue No. AC2–196 to be effective 1/18/2018. Filed Date: 1/25/18. Accession Number: 20180125–5047. Comments Due: 5 p.m. ET 2/15/18. The filings are accessible in the Commission’s eLibrary system by clicking on the links or querying the docket number. Any person desiring to intervene or protest in any of the above proceedings must file in accordance with Rules 211 and 214 of the Commission’s Regulations (18 CFR 385.211 and 385.214) on or before 5:00 p.m. Eastern time on the specified comment date. Protests may be considered, but intervention is necessary to become a party to the proceeding. VerDate Sep<11>2014 17:36 Jan 30, 2018 Jkt 244001 eFiling is encouraged. More detailed information relating to filing requirements, interventions, protests, service, and qualifying facilities filings can be found at: https://www.ferc.gov/ docs-filing/efiling/filing-req.pdf. For other information, call (866) 208–3676 (toll free). For TTY, call (202) 502–8659. Dated: January 25, 2018. Nathaniel J. Davis, Sr., Deputy Secretary. [FR Doc. 2018–01843 Filed 1–30–18; 8:45 am] BILLING CODE 6717–01–P ENVIRONMENTAL PROTECTION AGENCY [EPA–HQ–OW–2002–0011; FRL–9973–14– OEI] Information Collection Request Submitted to OMB for Review and Approval; Comment Request; Laboratory Quality Assurance Evaluation Program for Analysis of Cryptosporidium Under the Safe Drinking Water Act (Renewal) Environmental Protection Agency (EPA). ACTION: Notice. AGENCY: The Environmental Protection Agency has submitted an information collection request (ICR)—Laboratory Quality Assurance Evaluation Program for Analysis of Cryptosporidium Under the Safe Drinking Water Act, EPA ICR No. 2067.06, OMB Control No. 2040– 0246—to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act. This is a proposed extension of the ICR, which is currently approved through March 31, 2018. Public comments were previously requested via the Federal Register on October 16, 2017, during a 60-day comment period. This notice allows for an additional 30 days for public comments. A fuller description of the ICR is given below, including its estimated burden and cost to the public. An agency may not conduct or sponsor and a person is not required to respond to a collection of information unless it displays a currently valid OMB control number. DATES: Additional comments may be submitted on or before March 2, 2018. ADDRESSES: Submit your comments, referencing Docket ID No. EPA–HQ– OW–2002–0011, to (1) EPA online using www.regulations.gov (our preferred method), by email to ow-docket@ epa.gov, or by mail to: EPA Docket Center, Environmental Protection Agency, Mail Code 28221T, 1200 SUMMARY: PO 00000 Frm 00016 Fmt 4703 Sfmt 4703 Pennsylvania Ave., NW, Washington, DC 20460, and (2) OMB via email to oira_submission@omb.eop.gov. Address comments to OMB Desk Officer for EPA. EPA’s policy is that all comments received will be included in the public docket without change including any personal information provided, unless the comment includes profanity, threats, information claimed to be Confidential Business Information (CBI) or other information whose disclosure is restricted by statute. FOR FURTHER INFORMATION CONTACT: Dan Hautman, Technical Support Center (TSC), Office of Ground Water and Drinking Water, (MC–140), Environmental Protection Agency, 26 West Martin Luther King Drive, Cincinnati, Ohio 45268; telephone number: 513–569–7274; fax number: 513–569–7191; email address: Hautman.dan@epa.gov. SUPPLEMENTARY INFORMATION: Supporting documents, which explain in detail the information that the EPA will be collecting, are available in the public docket for this ICR. The docket can be viewed online at www.regulations.gov or in person at the EPA Docket Center, WJC West, Room 3334, 1301 Constitution Ave. NW, Washington, DC. The telephone number for the Docket Center is 202–566–1744. For additional information about EPA’s public docket, visit https://www.epa.gov/ dockets. Abstract: Under the Long Term 2 Enhanced Surface Water Treatment Rule (LT2ESWTR), EPA requires public water systems (PWS) to use approved laboratories when conducting Cryptosporidium monitoring. The Code of Federal Regulations (CFR) at 40 CFR 141.705(a) provides for approval of Cryptosporidium laboratories by ‘‘an equivalent’’ state laboratory certification program (i.e., equivalent to EPA’s Laboratory Quality Assurance Evaluation Program). In the preamble to the LT2ESWTR as well as several other notices, EPA has described the criteria for approval of laboratories to analyze Cryptosporidium samples under the LT2ESWTR. Form Numbers: None. Respondents/affected entities: Interested states and laboratories. Respondent’s obligation to respond: Voluntary. Estimated number of respondents: 43 labs and 20 states/territories. Frequency of response: Annual. Total estimated burden: 3,741 hours (per year). Burden is defined at 5 CFR 1320.03(b). Total estimated cost: $669,490, includes $332,891 annualized capital or operation & maintenance (O&M) costs. E:\FR\FM\31JAN1.SGM 31JAN1 Federal Register / Vol. 83, No. 21 / Wednesday, January 31, 2018 / Notices Changes in Estimates: There is a decrease of 1,731 hours and $134,284 in the total estimated respondent burden compared with the ICR currently approved by OMB. This decrease is due to a reduced number of laboratories (45 to 43), re-evaluation of hours for tasks, and an improved demonstration of capability by the laboratories. Courtney Kerwin, Director, Regulatory Support Division. [FR Doc. 2018–01899 Filed 1–30–18; 8:45 am] BILLING CODE 6560–50–P ENVIRONMENTAL PROTECTION AGENCY [EPA–HQ–ORD–2017–0474; FRL–9973–13– ORD] Availability of the Integrated Risk Information System (IRIS) Assessment Plan for Uranium Environmental Protection Agency (EPA). ACTION: Notice of public comment period. AGENCY: The Environmental Protection Agency (EPA) is announcing a 30-day public comment period associated with release of the draft IRIS Assessment Plan for Uranium. This document communicates information on the scoping needs identified by EPA program and regional offices and the IRIS Program’s initial problem formulation activities. Specifically, the assessment plan outlines the objectives for each assessment and the type of evidence considered most pertinent to address the scoping needs. EPA is releasing this draft IRIS Assessment Plan for public comment at least 60 days in advance of a public science webinar planned on March 22, 2018. DATES: The 30-day public comment period begins January 31, 2018, and ends March 2, 2018. Comments must be received on or before March 2, 2018. ADDRESSES: The IRIS Assessment Plan for Uranium, will be available via the internet on IRIS’ website at https:// cfpub.epa.gov/ncea/iris2/chemical Landing.cfm?substance_nmbr=259 and in the public docket at https:// www.regulations.gov, Docket ID: EPA– HQ–ORD–2017–0474. FOR FURTHER INFORMATION CONTACT: For information on the public comment period, contact the ORD Docket at the EPA Headquarters Docket Center; telephone: 202–566–1752; facsimile: 202–566–9744; or email: Docket_ORD@ epa.gov. For technical information on the draft IRIS Assessment Plan for Uranium, sradovich on DSK3GMQ082PROD with NOTICES SUMMARY: VerDate Sep<11>2014 17:36 Jan 30, 2018 Jkt 244001 contact Dr. James Avery, NCEA; telephone: 202–564–1494; or email: avery.james@epa.gov. SUPPLEMENTARY INFORMATION: I. Background Information on IRIS Assessment Plans EPA’s IRIS Program is a human health assessment program that evaluates quantitative and qualitative risk information on effects that may result from exposure to chemicals found in the environment. Through the IRIS Program, EPA provides the highest quality science-based human health assessments to support the Agency’s regulatory activities and decisions to protect public health. As part of scoping and initial problem formulation activities prior to the development of a draft assessment, the IRIS Program carries out a broad, preliminary literature survey to assist in identifying health effects that have been studied in relation to the chemical or substance of interest, as well as science issues that may need to be considered when evaluating toxicity. This information, in conjunction with scoping needs identified by EPA program and regional offices, is used to inform the development of an IRIS Assessment Plan (IAP). The IAP communicates the plan for developing each individual chemical assessment to the public and includes summary information on the IRIS Program’s scoping and initial problem formulation, objectives and specific aims for the assessment, and a PECO (Populations, Exposures, Comparators, and Outcomes) for the systematic review. The PECO provides the framework for developing literature search strategies and inclusion/ exclusion criteria, particularly with respect to evidence stream (i.e., human, animal, mechanistic), exposure measures and outcome measures. The IAP serves to inform the subsequent development of chemical-specific systematic review protocols, which will be made publicly available. II. Public Webinar In order to allow for public input, EPA is convening a public webinar to discuss the draft IRIS Assessment Plan for Uranium March 22, 2018. Specific teleconference and webinar information regarding this public meeting will be provided through the IRIS website (https://www.epa.gov/iris) and via EPA’s Human Health Risk Assessment (HHRA) and IRIS listservs. To register for the HHRA or IRIS listserv, visit the IRIS website (https://www.epa.gov/iris) or visit https://www.epa.gov/iris/forms/ PO 00000 Frm 00017 Fmt 4703 Sfmt 4703 4479 staying-connected-integrated-riskinformation-system#connect. III. How To Submit Technical Comments to the Docket at https:// www.regulations.gov Submit your comments, identified by Docket ID No. EPA–HQ–ORD–2017– 0474 for uranium, by one of the following methods: • www.regulations.gov: Follow the on-line instructions for submitting comments. • Email: Docket_ORD@epa.gov. • Fax: 202–566–9744. • Mail: U.S. Environmental Protection Agency, EPA Docket Center (ORD Docket), Mail Code: 28221T, 1200 Pennsylvania Avenue NW, Washington, DC 20460. The phone number is 202– 566–1752. • Hand Delivery: The ORD Docket is located in the EPA Headquarters Docket Center, EPA West Building, Room 3334, 1301 Constitution Avenue NW, Washington, DC 20229. The EPA Docket Center Public Reading Room is open from 8:30 a.m. to 4:30 p.m., Monday through Friday, excluding legal holidays. The telephone number for the Public Reading Room is 202–566–1744. Deliveries are only accepted during the docket’s normal hours of operation, and special arrangements should be made for deliveries of boxed information. If you provide comments by mail or hand delivery, please submit three copies of the comments. For attachments, provide an index, number pages consecutively with the comments, and submit an unbound original and three copies. Instructions: Direct your comments to docket number EPA–HQ–ORD–2017– 0474 for uranium. Please ensure that your comments are submitted within the specified comment period. Comments received after the closing date will be marked ‘‘late,’’ and may only be considered if time permits. It is EPA’s policy to include all comments it receives in the public docket without change and to make the comments available online at www.regulations.gov, including any personal information provided, unless a comment includes information claimed to be Confidential Business Information (CBI) or other information for which disclosure is restricted by statute. Do not submit information through www.regulations.gov or email that you consider to be CBI or otherwise protected. The www.regulations.gov website is an ‘‘anonymous access’’ system, which means EPA will not know your identity or contact information unless you provide it in the body of your comment. If you send an E:\FR\FM\31JAN1.SGM 31JAN1

Agencies

[Federal Register Volume 83, Number 21 (Wednesday, January 31, 2018)]
[Notices]
[Pages 4478-4479]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-01899]


=======================================================================
-----------------------------------------------------------------------

ENVIRONMENTAL PROTECTION AGENCY

[EPA-HQ-OW-2002-0011; FRL-9973-14-OEI]


Information Collection Request Submitted to OMB for Review and 
Approval; Comment Request; Laboratory Quality Assurance Evaluation 
Program for Analysis of Cryptosporidium Under the Safe Drinking Water 
Act (Renewal)

AGENCY: Environmental Protection Agency (EPA).

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: The Environmental Protection Agency has submitted an 
information collection request (ICR)--Laboratory Quality Assurance 
Evaluation Program for Analysis of Cryptosporidium Under the Safe 
Drinking Water Act, EPA ICR No. 2067.06, OMB Control No. 2040-0246--to 
the Office of Management and Budget (OMB) for review and approval in 
accordance with the Paperwork Reduction Act. This is a proposed 
extension of the ICR, which is currently approved through March 31, 
2018. Public comments were previously requested via the Federal 
Register on October 16, 2017, during a 60-day comment period. This 
notice allows for an additional 30 days for public comments. A fuller 
description of the ICR is given below, including its estimated burden 
and cost to the public. An agency may not conduct or sponsor and a 
person is not required to respond to a collection of information unless 
it displays a currently valid OMB control number.

DATES: Additional comments may be submitted on or before March 2, 2018.

ADDRESSES: Submit your comments, referencing Docket ID No. EPA-HQ-OW-
2002-0011, to (1) EPA online using www.regulations.gov (our preferred 
method), by email to [email protected], or by mail to: EPA Docket 
Center, Environmental Protection Agency, Mail Code 28221T, 1200 
Pennsylvania Ave., NW, Washington, DC 20460, and (2) OMB via email to 
[email protected]. Address comments to OMB Desk Officer for 
EPA.
    EPA's policy is that all comments received will be included in the 
public docket without change including any personal information 
provided, unless the comment includes profanity, threats, information 
claimed to be Confidential Business Information (CBI) or other 
information whose disclosure is restricted by statute.

FOR FURTHER INFORMATION CONTACT: Dan Hautman, Technical Support Center 
(TSC), Office of Ground Water and Drinking Water, (MC-140), 
Environmental Protection Agency, 26 West Martin Luther King Drive, 
Cincinnati, Ohio 45268; telephone number: 513-569-7274; fax number: 
513-569-7191; email address: [email protected].

SUPPLEMENTARY INFORMATION: Supporting documents, which explain in 
detail the information that the EPA will be collecting, are available 
in the public docket for this ICR. The docket can be viewed online at 
www.regulations.gov or in person at the EPA Docket Center, WJC West, 
Room 3334, 1301 Constitution Ave. NW, Washington, DC. The telephone 
number for the Docket Center is 202-566-1744. For additional 
information about EPA's public docket, visit https://www.epa.gov/dockets.
    Abstract: Under the Long Term 2 Enhanced Surface Water Treatment 
Rule (LT2ESWTR), EPA requires public water systems (PWS) to use 
approved laboratories when conducting Cryptosporidium monitoring. The 
Code of Federal Regulations (CFR) at 40 CFR 141.705(a) provides for 
approval of Cryptosporidium laboratories by ``an equivalent'' state 
laboratory certification program (i.e., equivalent to EPA's Laboratory 
Quality Assurance Evaluation Program). In the preamble to the LT2ESWTR 
as well as several other notices, EPA has described the criteria for 
approval of laboratories to analyze Cryptosporidium samples under the 
LT2ESWTR.
    Form Numbers: None.
    Respondents/affected entities: Interested states and laboratories.
    Respondent's obligation to respond: Voluntary.
    Estimated number of respondents: 43 labs and 20 states/territories.
    Frequency of response: Annual.
    Total estimated burden: 3,741 hours (per year). Burden is defined 
at 5 CFR 1320.03(b).
    Total estimated cost: $669,490, includes $332,891 annualized 
capital or operation & maintenance (O&M) costs.

[[Page 4479]]

    Changes in Estimates: There is a decrease of 1,731 hours and 
$134,284 in the total estimated respondent burden compared with the ICR 
currently approved by OMB. This decrease is due to a reduced number of 
laboratories (45 to 43), re-evaluation of hours for tasks, and an 
improved demonstration of capability by the laboratories.

Courtney Kerwin,
Director, Regulatory Support Division.
[FR Doc. 2018-01899 Filed 1-30-18; 8:45 am]
 BILLING CODE 6560-50-P


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