Coordination of Protection Systems for Performance During Faults and Specific Training for Personnel Reliability Standards, 56759 [C1-2017-25586]

Download as PDF Federal Register / Vol. 82, No. 229 / Thursday, November 30, 2017 / Proposed Rules • CSU retail sales or shipments, especially information about the type of CSUs sold and the number of units sold in recent years; • the number of CSUs in use; • studies, tests, or descriptions of technologies or design changes that address tip-over injuries and estimates of costs associated with those features, including manufacturing costs and wholesale prices; • the expected impact of technologies or design changes that address tip-over injuries on manufacturing costs or wholesale prices; • the potential impact of design changes to address CSU stability on consumer utility; and • information about whether any stability requirements for CSUs in ether a voluntary standard or potential mandatory rule could have a disparate impact on small entities, such as small manufacturers or importers. In addition, the Commission invites interested parties to submit any existing standards, or portions of them, for consideration as a consumer product safety standard. The Commission also invites interested persons to submit a statement of intention to modify or develop a voluntary consumer product safety standard addressing the risk of injury associated with CSU tip overs, including a description of the plan to develop or modify such a standard. Please submit comments in accordance with the instructions in the ADDRESSES section at the beginning of this ANPR. Alberta E. Mills, Acting Secretary, Consumer Product Safety Commission. [FR Doc. 2017–25779 Filed 11–29–17; 8:45 am] BILLING CODE 6355–01–P DEPARTMENT OF ENERGY Federal Energy Regulatory Commission 18 CFR Part 40 nshattuck on DSK9F9SC42PROD with PROPOSALS [Docket No. RM16–22–000] Coordination of Protection Systems for Performance During Faults and Specific Training for Personnel Reliability Standards Correction Proposed Rule document 2017–25586 beginning on page 56186 was incorrectly published in the issue of Tuesday, November 28, 2017. [FR Doc. C1–2017–25586 Filed 11–29–17; 8:45 am] BILLING CODE 1505–01–D VerDate Sep<11>2014 15:27 Nov 29, 2017 Jkt 244001 DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration 21 CFR Part 15 [Docket No. FDA–2017–N–6529] The Food and Drug Administration’s Approach To Evaluating Nicotine Replacement Therapies; Public Hearing; Request for Comments AGENCY: Food and Drug Administration, HHS. Notification of public hearing; request for comments. ACTION: The Food and Drug Administration (FDA or the Agency) is announcing a public hearing on FDA’s approach to evaluating the safety and efficacy of nicotine replacement therapy (NRT) products, including how they should be used and labeled. DATES: The public hearing will be held on Friday, January 26, 2018, from 9 a.m. to 5 p.m. The public hearing may be extended or may end early depending on the level of public participation. Persons seeking to attend or to present at the public hearing must register by Tuesday, January 2, 2018. Section II provides attendance and registration information. Electronic or written comments will be accepted after the public hearing until Thursday, February 15, 2018. ADDRESSES: The public hearing will be held at the FDA White Oak Campus, 10903 New Hampshire Ave., Bldg. 31 Conference Center, the Great Room A, Silver Spring, MD 20993–0002. Entrance for public hearing participants (non-FDA employees) is through Building 1 where routine security check procedures will be performed. For parking and security information, please refer to https://www.fda.gov/AboutFDA/ WorkingatFDA/BuildingsandFacilities/ WhiteOakCampusInformation/ ucm241740.htm. You may submit comments as follows. Please note that late, untimely filed comments will not be considered. Electronic comments must be submitted on or before February 15, 2018. The https://www.regulations.gov electronic filing system will accept comments until midnight Eastern Time at the end of February 15, 2018. Comments received by mail/hand delivery/courier (for written/paper submissions) will be considered timely if they are postmarked or the delivery service acceptance receipt is on or before that date. You may submit comments as follows: SUMMARY: PO 00000 Frm 00011 Fmt 4702 Sfmt 4702 56759 Electronic Submissions Submit electronic comments in the following way: • Federal eRulemaking Portal: https://www.regulations.gov. Follow the instructions for submitting comments. Comments submitted electronically, including attachments, to https:// www.regulations.gov will be posted to the docket unchanged. Because your comment will be made public, you are solely responsible for ensuring that your comment does not include any confidential information that you or a third party may not wish to be posted, such as medical information, your or anyone else’s Social Security number, or confidential business information, such as a manufacturing process. Please note that if you include your name, contact information, or other information that identifies you in the body of your comments, that information will be posted on https://www.regulations.gov. • If you want to submit a comment with confidential information that you do not wish to be made available to the public, submit the comment as a written/paper submission and in the manner detailed (see ‘‘Written/Paper Submissions’’ and ‘‘Instructions’’). Written/Paper Submissions Submit written/paper submissions as follows: • Mail/Hand delivery/Courier (for written/paper submissions): Dockets Management Staff (HFA–305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. • For written/paper comments submitted to the Dockets Management Staff, FDA will post your comment, as well as any attachments, except for information submitted, marked, and identified as confidential if submitted as detailed in ‘‘Instructions.’’ Instructions: All submissions received must include the Docket No. FDA– 2017–N–6529 for ‘‘FDA’s Approach to Evaluating Nicotine Replacement Therapies’’; Public Hearing; Request for Comments. Received comments will be placed in the docket and, except for those submitted as ‘‘Confidential Submissions,’’ publicly viewable at https://www.regulations.gov or at the Division of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday. • Confidential Submissions—To submit a comment with confidential information that you do not wish to be made publicly available, submit your comments only as a written/paper submission. You should submit two copies total. One copy will include the information you claim to be confidential E:\FR\FM\30NOP1.SGM 30NOP1

Agencies

[Federal Register Volume 82, Number 229 (Thursday, November 30, 2017)]
[Proposed Rules]
[Page 56759]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: C1-2017-25586]


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DEPARTMENT OF ENERGY

Federal Energy Regulatory Commission

18 CFR Part 40

[Docket No. RM16-22-000]


Coordination of Protection Systems for Performance During Faults 
and Specific Training for Personnel Reliability Standards

Correction

    Proposed Rule document 2017-25586 beginning on page 56186 was 
incorrectly published in the issue of Tuesday, November 28, 2017.

[FR Doc. C1-2017-25586 Filed 11-29-17; 8:45 am]
 BILLING CODE 1505-01-D