Agency Information Collection Activities: Proposed eCollection, eComments Requested; Reinstatement of a Discontinued Collection: Recordkeeping for Electronic Prescriptions for Controlled Substances, 58960 [2021-23208]

Download as PDF 58960 Federal Register / Vol. 86, No. 203 / Monday, October 25, 2021 / Notices Square, 145 N Street NE, 3E.405B, Washington, DC 20530. Dated: October 20, 2021. Melody Braswell, Department Clearance Officer for PRA, U.S. Department of Justice. [FR Doc. 2021–23209 Filed 10–22–21; 8:45 am] BILLING CODE 4410–18–P DEPARTMENT OF JUSTICE [OMB Number 1117–0049] Agency Information Collection Activities: Proposed eCollection, eComments Requested; Reinstatement of a Discontinued Collection: Recordkeeping for Electronic Prescriptions for Controlled Substances Drug Enforcement Administration, Department of Justice. ACTION: 30-Day notice. AGENCY: The Department of Justice (DOJ), Drug Enforcement Administration (DEA), will be submitting the following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act of 1995. DATES: Comments are encouraged and will be accepted for 30 days until November 24, 2021. FOR FURTHER INFORMATION CONTACT: 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. SUPPLEMENTARY INFORMATION: Written comments and suggestions from the SUMMARY: public and affected agencies concerning the proposed collection of information are encouraged. Your comments should address one or more of the following four points: —Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility; —Evaluate the accuracy of the agency’s estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; —Evaluate whether and if so how the quality, utility, and clarity of the information proposed to be collected can be enhanced; and —Minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated, electronic, mechanical, or other forms of information technology, e.g., permitting electronic submission of responses. 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 requires that each registered practitioner apply to an approved credential service provider 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 permission 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 conducts 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. jspears on DSK121TN23PROD with NOTICES1 Number of respondents Hour burden per response 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, VerDate Sep<11>2014 18:00 Oct 22, 2021 Jkt 256001 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. PO 00000 Frm 00102 Fmt 4703 Sfmt 9990 Dated: October 20, 2021. Melody Braswell, Department Clearance Officer for PRA, U.S. Department of Justice. [FR Doc. 2021–23208 Filed 10–22–21; 8:45 am] BILLING CODE 4410–09–P E:\FR\FM\25OCN1.SGM 25OCN1

Agencies

[Federal Register Volume 86, Number 203 (Monday, October 25, 2021)]
[Notices]
[Page 58960]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-23208]


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DEPARTMENT OF JUSTICE

[OMB Number 1117-0049]


Agency Information Collection Activities: Proposed eCollection, 
eComments Requested; Reinstatement of a Discontinued Collection: 
Recordkeeping for Electronic Prescriptions for Controlled Substances

AGENCY: Drug Enforcement Administration, Department of Justice.

ACTION: 30-Day notice.

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

SUMMARY: The Department of Justice (DOJ), Drug Enforcement 
Administration (DEA), will be submitting the following information 
collection request to the Office of Management and Budget (OMB) for 
review and approval in accordance with the Paperwork Reduction Act of 
1995.

DATES:  Comments are encouraged and will be accepted for 30 days until 
November 24, 2021.

FOR FURTHER INFORMATION CONTACT:  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.

SUPPLEMENTARY INFORMATION:  Written comments and suggestions from the 
public and affected agencies concerning the proposed collection of 
information are encouraged. Your comments should address one or more of 
the following four points:
--Evaluate whether the proposed collection of information is necessary 
for the proper performance of the functions of the agency, including 
whether the information will have practical utility;
--Evaluate the accuracy of the agency's estimate of the burden of the 
proposed collection of information, including the validity of the 
methodology and assumptions used;
--Evaluate whether and if so how the quality, utility, and clarity of 
the information proposed to be collected can be enhanced; and
--Minimize the burden of the collection of information on those who are 
to respond, including through the use of appropriate automated, 
electronic, mechanical, or other forms of information technology, e.g., 
permitting electronic submission of responses.

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 requires that each registered practitioner apply to 
an approved credential service provider 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 permission 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 
conducts 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      Hour burden
                                                                    respondents    per response    Burden hours
----------------------------------------------------------------------------------------------------------------
Practitioners...................................................          78,164            0.67          52,370
MLP.............................................................          49,067            0.67          32,875
Hospital/Clinics................................................           1,482            2.13           3,157
Pharmacies......................................................           3,984            0.33           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: October 20, 2021.
Melody Braswell,
Department Clearance Officer for PRA, U.S. Department of Justice.
[FR Doc. 2021-23208 Filed 10-22-21; 8:45 am]
BILLING CODE 4410-09-P
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