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Federal Register / Vol. 86, No. 156 / Tuesday, August 17, 2021 / Notices Overview of This Information Collection 1. Type of Information Collection:
Reinstatement of a discontinued collection.
2. Title of the Form/Collection:
Recordkeeping for Electronic Prescriptions for Controlled Substance.
3. The agency form number, if any, and the applicable component of the Department sponsoring the collection:
There is no form number. The applicable component within the Department of Justice is the Drug Enforcement Administration, Diversion Control Division.
4. Affected public who will be asked or required to respond, as well as a brief abstract:
Affected public Primary: Business or other for-profit.
Affected public Other: Not-for-profit institutions; Federal, State, local, and tribal governments.

Abstract: DEA is requiring that each registered practitioner apply to an approved credential service provider approved to obtain identity proofing and a credential. Hospitals and other institutional practitioners may conduct this process in-house as part of their credentialing. For practitioners currently working at or affiliated with a registered hospital or clinic, the hospital/clinic have to check a government-issued photographic identification. This may be done when the hospital/clinic issues credentials to new hires or newly affiliated physicians. For individual practitioners, two people need to enter logical access control data to grant permissions for practitioners authorized to approve and sign controlled substance prescriptions using the electronic prescription application. For institutional practitioners, logical access control data is entered by two people from an entity
within the hospital/clinic that is separate from the entity that conduct identity proofing in-house. Similarly, pharmacies have to set logical access controls in the pharmacy application so that only authorized employees have permission to annotate or alter prescription records. Finally, if the electronic prescription or pharmacy application generates an incident report, practitioners, hospitals/clinics, and pharmacies have to review the incident report to determine if the event identified by the application represents a security incident.
5. An estimate of the total number of respondents and the amount of time estimated for an average respondent to respond: The below table presents information regarding the number of respondents, hour burden per responses and associated burden hours.
Number of respondents
Burden hours
Practitioners
MLP
Hospital/Clinics
Pharmacies

78,164
49,067
1,482
3,984

0.67
0.67
2.13
0.33

52,370
32,875
3,157
1,315

Total

132,697

89,717

6. An estimate of the total public burden in hours associated with the proposed collection: DEA estimates that this collection takes 89,717 annual burden hours.
If additional information is required please contact: Melody Braswell, Department Clearance Officer, United States Department of Justice, Justice Management Division, Policy and Planning Staff, Two Constitution Square, 145 N Street NE, Suite 3E.405B, Washington, DC 20530.
Dated: August 11, 2021.
Melody Braswell, Department Clearance Officer for PRA, U.S.
Department of Justice.
FR Doc. 202117523 Filed 81621; 8:45 am BILLING CODE 441009P

DEPARTMENT OF LABOR

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Hour burden per response
Agency Information Collection Activities; Submission for OMB
Review; Comment Request;
Respiratory Protection Standard Notice of availability; request for comments.

ACTION:

The Department of Labor DOL is submitting this Occupational
SUMMARY:

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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 September 16, 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 ReviewOpen 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 agencys estimates of the burden and cost of the collection of information, including the validity of the methodology and assumptions used; 4

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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
6930456 or by email at DOL_PRA_
PUBLIC@dol.gov.
SUPPLEMENTARY INFORMATION: This standard requires employers to develop a written respiratory protection program, provide medical surveillance, fit test employees, obtain certificates of analysis on cylinders, change sorbent beds and filters, to inspect emergencyuse respirators, mark emergency-use respirator storage compartments, and maintain accurate employee records for fit testing and medical surveillance. For additional substantive information about this ICR, see the related notice published in the Federal Register on April 9, 2021 86 FR 18557.
This information collection is subject to the PRA. A Federal agency generally 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
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