Bulk Manufacturer of Controlled Substances Application: PCI Synthesis, 53117 [2021-20762]

Download as PDF Federal Register / Vol. 86, No. 183 / Friday, September 24, 2021 / Notices business activity is consistent with what is authorized under 21 U.S.C. 952(a)(2). Agency Information Collection Activities; Submission for OMB Review; Comment Request; PermitRequired Confined Spaces Brian S. Besser, Acting Assistant Administrator. [FR Doc. 2021–20760 Filed 9–23–21; 8:45 am] BILLING CODE P Notice of availability; request for comments. ACTION: DEPARTMENT OF JUSTICE [Docket No. DEA–896] Bulk Manufacturer of Controlled Substances Application: PCI Synthesis Drug Enforcement Administration, Justice. AGENCY: Notice of application. PCI Synthesis has applied to be registered as a bulk manufacturer of basic class(es) of controlled substance(s). Refer to Supplemental Information listed below for further drug information. SUMMARY: Registered bulk manufacturers of the affected basic class(es), and applicants therefore, may file written comments on or objections to the issuance of the proposed registration on or before November 23, 2021. Such persons may also file a written request for a hearing on the application on or before November 23, 2021. DATES: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia 22152. ADDRESSES: In accordance with 21 CFR 1301.33(a), this is notice that on March 30, 2021, PCI Synthesis, 9 Opportunity Way, Newburyport, Massachusetts 01950– 0195, applied to be registered as a bulk manufacturer of the following basic class(es) of controlled substance(s): SUPPLEMENTARY INFORMATION: Drug code Controlled substance Amphetamine ............... Methamphetamine ........ I Schedule 1100 1105 II III The company plans to develop manufacturing processes, conduct analytical method validation and conduct bulk product stability studies. Brian S. Besser, Acting Assistant Administrator. [FR Doc. 2021–20762 Filed 9–23–21; 8:45 am] BILLING CODE P VerDate Sep<11>2014 16:50 Sep 23, 2021 The Department of Labor (DOL) is submitting this Occupational Safety and Health Administration (OSHA)-sponsored information collection request (ICR) to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act of 1995 (PRA). Public comments on the ICR are invited. DATES: The OMB will consider all written comments that agency receives on or before October 25, 2021. ADDRESSES: Written comments and recommendations for the proposed information collection should be sent within 30 days of publication of this notice to www.reginfo.gov/public/do/ PRAMain. Find this particular information collection by selecting ‘‘Currently under 30-day Review—Open for Public Comments’’ or by using the search function. Comments are invited on: (1) Whether the collection of information is necessary for the proper performance of the functions of the Department, including whether the information will have practical utility; (2) if the information will be processed and used in a timely manner; (3) the accuracy of the agency’s estimates of the burden and cost of the collection of information, including the validity of the methodology and assumptions used; (4) ways to enhance the quality, utility and clarity of the information collection; and (5) ways to minimize the burden of the collection of information on those who are to respond, including the use of automated collection techniques or other forms of information technology. FOR FURTHER INFORMATION CONTACT: Crystal Rennie by telephone at 202– 693–0456 or by email at DOL_PRA_ PUBLIC@dol.gov. SUPPLEMENTARY INFORMATION: The collections of information are needed by employers and employees involved in the entry of permit-required confined spaces to prevent injuries and death from exposure to the hazards associated with such entries. For additional substantive information about this ICR, see the related notice published in the Federal Register on June 23, 2021 (86 FR 32978). This information collection is subject to the PRA. A Federal agency generally SUMMARY: Drug Enforcement Administration ACTION: DEPARTMENT OF LABOR Jkt 253001 PO 00000 Frm 00090 Fmt 4703 Sfmt 4703 53117 cannot conduct or sponsor a collection of information, and the public is generally not required to respond to an information collection, unless the OMB approves it and displays a currently valid OMB Control Number. In addition, notwithstanding any other provisions of law, no person shall generally be subject to penalty for failing to comply with a collection of information that does not display a valid OMB Control Number. See 5 CFR 1320.5(a) and 1320.6. DOL seeks PRA authorization for this information collection for three (3) years. OMB authorization for an ICR cannot be for more than three (3) years without renewal. The DOL notes that information collection requirements submitted to the OMB for existing ICRs receive a month-to-month extension while they undergo review. Agency: DOL–OSHA. Title of Collection: Permit-Required Confined Spaces. OMB Control Number: 1218–0203. Affected Public: Private Sector: Businesses or other for-profits. Total Estimated Number of Respondents: 214,994. Total Estimated Number of Responses: 13,959,314. Total Estimated Annual Time Burden: 2,076,039 hours. Total Estimated Annual Other Costs Burden: $645,000. Authority: 44 U.S.C. 3507(a)(1)(D). Crystal Rennie, Senior PRA Analyst. [FR Doc. 2021–20729 Filed 9–23–21; 8:45 am] BILLING CODE 4510–26–P NATIONAL AERONAUTICS AND SPACE ADMINISTRATION [Notice: (21–061)] Planetary Science Advisory Committee; Meeting National Aeronautics and Space Administration. ACTION: Notice of meeting. AGENCY: In accordance with the Federal Advisory Committee Act, as amended, the National Aeronautics and Space Administration (NASA) announces a meeting of the Planetary Science Advisory Committee. The meeting will be held for the purpose of soliciting, from the scientific community and other persons, scientific and technical information relevant to program planning. DATES: Monday, October 18, 2021, 10:00 a.m. to 6:00 p.m., Eastern Time; and Tuesday, October 19, 2021, 10:00 a.m. to 6:00 p.m., Eastern Time SUMMARY: E:\FR\FM\24SEN1.SGM 24SEN1

Agencies

[Federal Register Volume 86, Number 183 (Friday, September 24, 2021)]
[Notices]
[Page 53117]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-20762]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-896]


Bulk Manufacturer of Controlled Substances Application: PCI 
Synthesis

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application.

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SUMMARY: PCI Synthesis has applied to be registered as a bulk 
manufacturer of basic class(es) of controlled substance(s). Refer to 
Supplemental Information listed below for further drug information.

DATES: Registered bulk manufacturers of the affected basic class(es), 
and applicants therefore, may file written comments on or objections to 
the issuance of the proposed registration on or before November 23, 
2021. Such persons may also file a written request for a hearing on the 
application on or before November 23, 2021.

ADDRESSES: Written comments should be sent to: Drug Enforcement 
Administration, Attention: DEA Federal Register Representative/DPW, 
8701 Morrissette Drive, Springfield, Virginia 22152.

SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.33(a), this 
is notice that on March 30, 2021, PCI Synthesis, 9 Opportunity Way, 
Newburyport, Massachusetts 01950-0195, applied to be registered as a 
bulk manufacturer of the following basic class(es) of controlled 
substance(s):

------------------------------------------------------------------------
                                           Drug
          Controlled substance             code          Schedule
------------------------------------------------------------------------
Amphetamine............................     1100  II
Methamphetamine........................     1105  II
------------------------------------------------------------------------

    The company plans to develop manufacturing processes, conduct 
analytical method validation and conduct bulk product stability 
studies.

Brian S. Besser,
Acting Assistant Administrator.
[FR Doc. 2021-20762 Filed 9-23-21; 8:45 am]
BILLING CODE P
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