Agency Information Collection Activities: Submission for OMB Review; Comment Request, 39204-39206 [2020-13986]
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39204
Federal Register / Vol. 85, No. 126 / Tuesday, June 30, 2020 / Notices
khammond on DSKJM1Z7X2PROD with NOTICES
Kroll Laboratory Specialists, Inc.,
Scientific Testing Laboratories, Inc.;
Kroll Scientific Testing Laboratories,
Inc.)
Clinical Reference Laboratory, Inc., 8433
Quivira Road, Lenexa, KS 66215–
2802, 800–445–6917
Cordant Health Solutions, 2617 East L
Street, Tacoma, WA 98421, 800–442–
0438 (Formerly: STERLING Reference
Laboratories)
Desert Tox, LLC, 5425 E Bell Rd., Suite
125, Scottsdale, AZ 85254, 602–457–
5411/623–748–5045
DrugScan, Inc., 200 Precision Road,
Suite 200, Horsham, PA 19044, 800–
235–4890
Dynacare,* 245 Pall Mall Street,
London, ONT, Canada N6A 1P4, 519–
679–1630 (Formerly: GammaDynacare Medical Laboratories)
Upon finding a Canadian laboratory to
be qualified, HHS will recommend that
DOT certify the laboratory (Federal
Register, July 16, 1996) as meeting the
minimum standards of the Mandatory
Guidelines published in the Federal
Register on January 23, 2017 (82 FR
7920). After receiving DOT certification,
the laboratory will be included in the
monthly list of HHS-certified
laboratories and participate in the NLCP
certification maintenance program.
ElSohly Laboratories, Inc., 5 Industrial
Park Drive, Oxford, MS 38655, 662–
236–2609
Laboratory Corporation of America
Holdings, 7207 N. Gessner Road,
Houston, TX 77040, 713–856–8288/
800–800–2387
Laboratory Corporation of America
Holdings, 69 First Ave., Raritan, NJ
08869, 908–526–2400/800–437–4986,
(Formerly: Roche Biomedical
Laboratories, Inc.)
Laboratory Corporation of America
Holdings, 1904 TW Alexander Drive,
Research Triangle Park, NC 27709,
919–572–6900/800–833–3984,
(Formerly: LabCorp Occupational
Testing Services, Inc., CompuChem
Laboratories, Inc.; CompuChem
Laboratories, Inc., A Subsidiary of
* The Standards Council of Canada (SCC) voted
to end its Laboratory Accreditation Program for
Substance Abuse (LAPSA) effective May 12, 1998.
Laboratories certified through that program were
accredited to conduct forensic urine drug testing as
required by U.S. Department of Transportation
(DOT) regulations. As of that date, the certification
of those accredited Canadian laboratories will
continue under DOT authority. The responsibility
for conducting quarterly performance testing plus
periodic on-site inspections of those LAPSAaccredited laboratories was transferred to the U.S.
HHS, with the HHS’ NLCP contractor continuing to
have an active role in the performance testing and
laboratory inspection processes. Other Canadian
laboratories wishing to be considered for the NLCP
may apply directly to the NLCP contractor just as
U.S. laboratories do.
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18:18 Jun 29, 2020
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Roche Biomedical Laboratory; Roche
CompuChem Laboratories, Inc., A
Member of the Roche Group)
Laboratory Corporation of America
Holdings, 1120 Main Street,
Southaven, MS 38671, 866–827–8042/
800–233–6339, (Formerly: LabCorp
Occupational Testing Services, Inc.;
MedExpress/National Laboratory
Center)
LabOne, Inc. d/b/a Quest Diagnostics,
10101 Renner Blvd., Lenexa, KS
66219, 913–888–3927/800–873–8845,
(Formerly: Quest Diagnostics
Incorporated; LabOne, Inc.; Center for
Laboratory Services, a Division of
LabOne, Inc.)
Legacy Laboratory Services Toxicology,
1225 NE 2nd Ave., Portland, OR
97232, 503–413–5295/800–950–5295,
MedTox Laboratories, Inc., 402 W.
County Road D, St. Paul, MN 55112,
651–636–7466/800–832–3244
Minneapolis Veterans Affairs Medical
Center, Forensic Toxicology
Laboratory, 1 Veterans Drive,
Minneapolis, MN 55417, 612–725–
2088, Testing for Veterans Affairs
(VA) Employees Only.
Pacific Toxicology Laboratories, 9348
DeSoto Ave., Chatsworth, CA 91311,
800–328–6942, (Formerly: Centinela
Hospital Airport Toxicology
Laboratory)
Pathology Associates Medical
Laboratories, 110 West Cliff Dr.,
Spokane, WA 99204, 509–755–8991/
800–541–7891x7
Phamatech, Inc., 15175 Innovation
Drive, San Diego, CA 92128, 888–
635–5840
Quest Diagnostics Incorporated, 1777
Montreal Circle, Tucker, GA 30084,
800–729–6432, (Formerly: SmithKline
Beecham Clinical Laboratories;
SmithKline Bio-Science Laboratories)
Quest Diagnostics Incorporated, 400
Egypt Road, Norristown, PA 19403,
610–631–4600/877–642–2216,
(Formerly: SmithKline Beecham
Clinical Laboratories; SmithKline BioScience Laboratories)
Redwood Toxicology Laboratory, 3700
Westwind Blvd., Santa Rosa, CA
95403, 800–255–2159,
U.S. Army Forensic Toxicology Drug
Testing Laboratory, 2490 Wilson St.,
Fort George G. Meade, MD 20755–
5235, 301–677–7085, Testing for
Department of Defense (DoD)
Employees Only
Anastasia Marie Donovan,
Policy Analyst.
[FR Doc. 2020–14040 Filed 6–29–20; 8:45 am]
BILLING CODE 4162–20–P
PO 00000
Frm 00045
Fmt 4703
Sfmt 4703
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Substance Abuse and Mental Health
Services Administration
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Periodically, the Substance Abuse and
Mental Health Services Administration
(SAMHSA) will publish a summary of
information collection requests under
OMB review, in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
documents, call the SAMHSA Reports
Clearance Officer on (240) 276–0361.
Project: Mandatory Guidelines for
Federal Workplace Drug Testing
Programs (OMB No. 0930–0158)—
Revision
SAMHSA will request OMB approval
for a revision of the Federal Drug
Testing Custody and Control Form
(CCF) for Federal agency and federally
regulated drug testing programs which
must comply with the HHS Mandatory
Guidelines for Federal Workplace Drug
Testing Programs using Urine (UrMG)
dated January 23, 2017 (82 FR 7920) and
using Oral Fluid (OFMG) dated October
25, 2019, and OMB approval for
information provided by test facilities
(laboratories and Instrumented Initial
Test Facilities, IITFs) for the National
Laboratory Certification Program
(NLCP).
The CCF is used by all Federal
agencies and employers regulated by the
Department of Transportation (DOT)
and the Nuclear Regulatory Commission
(NRC) to document the collection and
chain of custody of urine specimens at
the collection site, for HHS-certified test
facilities to report results, and for
Medical Review Officers (MROs) to
document and report a verified result.
SAMHSA allows the use of the CCF as
a paper or electronic form.
The current OMB-approved CCF has
an August 31, 2020 expiration date.
SAMHSA has resubmitted the CCF with
revisions to the form for OMB approval.
During 60-day public comment 7
commenter’s submitted comments on
the proposed changes to the CCF. These
commenters were comprised of
individuals, organizations, and private
sector companies. All comments were
reviewed and taken into consideration
in the preparation of the revised CCF.
The issues and concerns raised in the
public comments for the CCF are set out
www.reginfo.gov/public/do/PRAMain.
These revisions are listed below:
E:\FR\FM\30JNN1.SGM
30JNN1
39205
Federal Register / Vol. 85, No. 126 / Tuesday, June 30, 2020 / Notices
Copies 1–5
Revised Step 1
1. Added ‘‘CDL State and No.’’ to donor
identification types
2. Added ‘‘Collector Contact Info:’’ and
‘‘Other’’ line (e.g., email)
Revised Step 2
1. Put Urine and Oral Fluid checkboxes
above Step 2 for collector to
annotate
2. Expanded to 4 lines for collector
entries:
—General entry for Split, Single, or
None Provided (same as current)
—Entries specific to urine collection
(moved ‘‘Collector reads urine
temperature within 4 minutes’’
here; other entries same as current)
—Entries specific to oral fluid
collection: Added ‘‘Split Type’’
with checkboxes for Serial,
Concurrent, and Subdivided; ‘‘Each
Device Within Expiration Date?’’
with checkboxes Yes or No; and
Volume Indicator(s) Observed
checkbox)
—Remarks (same as current)
Revised Step 3
1. Edited instruction to state ‘‘collector
affixes seal(s) to bottle(s)/tube(s)’’
Revised Step 4 (Collector Section)
1. Edited ‘‘Specimen Bottle(s) Released
To’’ box to state ‘‘Specimen
Bottle(s)/Tubes(s) Released To’’
Copy 1 (Test Facility Copy)
Revised Step 4 (Accessioner Section)
1. Edited ‘‘Specimen Bottle(s) Released
To’’ box to state ‘‘Specimen
Bottle(s)/Tubes(s) Released To’’
2. Added ‘‘Primary/Single Specimen
Device Expiration Date’’ and ‘‘Split
Specimen Device Expiration Date’’
fields for accessioner to annotate
expiration dates of oral fluid
collection devices
Revised Step 5a (Certification and
Reporting Section)
1. Removed analyte names and
checkboxes
2. Repositioned results and checkboxes:
Moved REJECTED FOR TESTING,
ADULTERATED, SUBSTITUTED
and INVALID RESULT checkboxes;
moved POSITIVE checkbox to be
under DILUTE
3. Added line for certifying scientist to
record positive analytes and
concentrations, and added
‘‘Analyte(s) in ng/mL’’ instruction
(aligned under ‘‘POSITIVE for:’’)
Copy 2 (Medical Review Officer Copy)
Revised Step 5 (Donor Section)
1. Added line for donor email address
2. Edited donor certification statement
to state ‘‘specimen bottle/tubes’’
Revised Step 6 (MRO section—Primary
Specimen)
1. Put Urine and Oral Fluid checkboxes
above Step 6 for MRO to annotate
Bottom of Copies
Revised Copy 1
1. Edited label/seal at bottom of Copy 1
to allow for modification (e.g.,
perforations, label with transparent
seal on one side, and separate label
and seal)
khammond on DSKJM1Z7X2PROD with NOTICES
Custody and Control Form: 1
Donor ............................................................................
Collector ........................................................................
Laboratory .....................................................................
IITF ................................................................................
Medical Review Officer .................................................
NLCP Application Form: 2
Laboratory .....................................................................
IITF ................................................................................
Sections B and C—NLCP Inspection Checklist:
Laboratory .....................................................................
IITF ................................................................................
Record Keeping:
Laboratory .....................................................................
IITF ................................................................................
Total .......................................................................
Written comments and
recommendations for the proposed
information collection should be sent
VerDate Sep<11>2014
18:18 Jun 29, 2020
Jkt 250001
Responses
per
respondent
Number of
respondents
Form/respondent
Frm 00046
1. Removed Instructions for Completing
the CCF from the back. SAMHSA
will post instructions for
completing the Federal CCF for
urine and oral fluid on their
website.
Based upon information from Federal
agencies and from DOT concerning their
regulated industries, the number of
respondents has increased from 5.4
million to 6.7 million, which increases
the total burden hours by 170,701.8–C;.
Laboratories and IITFs seeking HHS
certification under the NLCP must
complete and submit the NLCP
application form. The NLCP application
form has not been revised compared to
the previous form.
Prior to an inspection, an HHScertified laboratory or IITF is required to
submit specific information regarding
its procedures. Collecting this
information prior to an inspection
allows the inspectors to thoroughly
review and understand the testing
procedures before arriving for the onsite
inspection. The NLCP information
checklist has not been revised compared
to the previous form.
The annual total burden estimates for
the CCF, the NLCP application, the
NLCP information checklist, and the
NLCP recordkeeping requirements are
shown in the following table.
Total
number of
responses
Burden
per response
(hours)
Annual
burden
(hours)
6,726,610
6,726,610
6,726,610
1
6,726,610
1
1
1
0
1
6,726,610
6,726,610
6,726,610
0
6,726,610
0.08
0.07
0.05
0.05
0.05
538,128.8
378,000
336,330
0
270,000
5
0
5
0
5
0
3
3
15
0
29
0
1
0
29
0
1
1
29
0
29
0
1
0
29
0
250
250
7,250
0
6,726,673
........................
26,906,503
........................
1,529,753
within 30 days of publication of this
notice to www.reginfo.gov/public/do/
PRAMain. Find this particular
PO 00000
Revised Copy 5
Fmt 4703
Sfmt 4703
information collection by selecting
‘‘Currently under 30-day Review—Open
E:\FR\FM\30JNN1.SGM
30JNN1
39206
Federal Register / Vol. 85, No. 126 / Tuesday, June 30, 2020 / Notices
for Public Comments’’ or by using the
search function.
Carlos Graham,
Social Science Analyst.
[FR Doc. 2020–13986 Filed 6–29–20; 8:45 am]
BILLING CODE 4162–20–P
DEPARTMENT OF HOMELAND
SECURITY
U.S. Customs and Border Protection
[1651–0131]
Agency Information Collection
Activities: e-Allegations Submission
U.S. Customs and Border
Protection (CBP), Department of
Homeland Security.
ACTION: 60-Day notice and request for
comments; extension of an existing
collection of information.
AGENCY:
The Department of Homeland
Security, U.S. Customs and Border
Protection 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. The information
collection is published in the Federal
Register to obtain comments from the
public and affected agencies.
DATES: Comments are encouraged and
will be accepted no later than August
31, 2020 to be assured of consideration.
ADDRESSES: Written comments and/or
suggestions regarding the item(s)
contained in this notice must include
the OMB Control Number 1651–0131 in
the subject line and the agency name.
To avoid duplicate submissions, please
use only one of the following methods
to submit comments:
(1) Email. Submit comments to: CBP_
PRA@cbp.dhs.gov.
(2) Mail. Submit written comments to
CBP Paperwork Reduction Act Officer,
U.S. Customs and Border Protection,
Office of Trade, Regulations and
Rulings, Economic Impact Analysis
Branch, 90 K Street NE, 10th Floor,
Washington, DC 20229–1177.
FOR FURTHER INFORMATION CONTACT:
Requests for additional PRA information
should be directed to Seth Renkema,
U.S. Customs and Border Protection,
Office of Trade, Regulations and
Rulings, Economic Impact Analysis
Branch, 90 K Street NE, 10th Floor,
Washington, DC 20229–1177, or via
email CBP_PRA@cbp.dhs.gov. Please
note that the contact information
provided here is solely for questions
regarding this notice. Individuals
khammond on DSKJM1Z7X2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
18:18 Jun 29, 2020
Jkt 250001
seeking information about other CBP
programs should contact the CBP
National Customer Service Center at
877–227–5511, (TTY) 1–800–877–8339,
or CBP website at www.cbp.gov/.
SUPPLEMENTARY INFORMATION: CBP
invites the general public and other
Federal agencies to comment on the
proposed and/or continuing information
collections pursuant to the Paperwork
Reduction Act of 1995 (44 U.S.C. 3501
et seq.). This process is conducted in
accordance with 5 CFR 1320.8. Written
comments and suggestions from the
public and affected agencies should
address one or more of the following
four points: (1) 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; (2) 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; (3)
suggestions to enhance the quality,
utility, and clarity of the information to
be collected; and (4) suggestions to
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 technological
collection techniques or other forms of
information technology, e.g., permitting
electronic submission of responses. The
comments that are submitted will be
summarized and included in the request
for approval. All comments will become
a matter of public record.
Overview of This Information
Collection
Title: e-Allegations Submission.
OMB Number: 1651–0131.
Form Number: None.
Current Actions: CBP proposes to
extend the expiration date of this
information collection. There is no
change to the burden hours or to the
information collected.
Type of Review: Extension (without
change).
Affected Public: Businesses,
Individuals.
Abstract: In the interest of detecting
trade violations to customs laws,
Customs and Border Protection (CBP)
established the e-Allegations website to
provide a means for concerned members
of the trade community to confidentially
report violations to CBP. The eAllegations site allows the public to
submit pertinent information that assists
CBP in its decision whether or not to
pursue the alleged violations by
initiating an investigation. The
information collected includes the
PO 00000
Frm 00047
Fmt 4703
Sfmt 4703
name, phone number and email address
of the member of the trade community
reporting the alleged violation. It also
includes a description of the alleged
violation, and the name and address of
the potential violators. The eAllegations website is accessible at
https://apps.cbp.gov/eallegations/.
Estimated Number of Respondents:
1,600.
Estimated Number of Total Annual
Responses: 1,600.
Estimated Time per Response: 15
minutes.
Estimated Total Annual Burden
Hours: 400.
Dated: June 16, 2020.
Seth Renkema,
Branch Chief, Economic Impact Analysis
Branch, U.S. Customs and Border Protection.
[FR Doc. 2020–13295 Filed 6–29–20; 8:45 am]
BILLING CODE 9111–14–P
DEPARTMENT OF THE INTERIOR
Bureau of Land Management
[LLES00000.L51100000.GF0000.
LVEMM19M2070.19X]
Notice of Intent To Prepare an
Environmental Impact Statement for
the Twin Metals Project in the Superior
National Forest, Lake and St. Louis
Counties, Minnesota
Bureau of Land Management,
Interior.
ACTION: Notice of intent.
AGENCY:
In compliance with the
National Environmental Policy Act of
1969, as amended (NEPA), and the
Federal Land Policy and Management
Act of 1976 (FLPMA), as amended, the
Bureau of Land Management (BLM)
Northeastern States District, Milwaukee,
Wisconsin, intends to prepare an
Environmental Impact Statement (EIS)
to analyze the potential impacts of
issuing a proposed new preference right
lease (MNES 57965) and approving a
Mine Plan of Operation in the Superior
National Forest in Lake and St. Louis
Counties, Minnesota. The approval of a
Mine Plan of Operation allows the
lessee to access, and once other
necessary permits are obtained, to mine
federal minerals. The BLM will conduct
a public scoping process, including
public meetings. During this time, the
public will be invited to submit
comments.
SUMMARY:
The BLM will announce the
dates of public scoping, including dates
and locations of public meetings and the
ways in which people may submit
scoping comments, on its e-Planning
DATES:
E:\FR\FM\30JNN1.SGM
30JNN1
]]>Agencies
[Federal Register Volume 85, Number 126 (Tuesday, June 30, 2020)]
[Notices]
[Pages 39204-39206]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-13986]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Substance Abuse and Mental Health Services Administration
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
Periodically, the Substance Abuse and Mental Health Services
Administration (SAMHSA) will publish a summary of information
collection requests under OMB review, in compliance with the Paperwork
Reduction Act (44 U.S.C. Chapter 35). To request a copy of these
documents, call the SAMHSA Reports Clearance Officer on (240) 276-0361.
Project: Mandatory Guidelines for Federal Workplace Drug Testing
Programs (OMB No. 0930-0158)--Revision
SAMHSA will request OMB approval for a revision of the Federal Drug
Testing Custody and Control Form (CCF) for Federal agency and federally
regulated drug testing programs which must comply with the HHS
Mandatory Guidelines for Federal Workplace Drug Testing Programs using
Urine (UrMG) dated January 23, 2017 (82 FR 7920) and using Oral Fluid
(OFMG) dated October 25, 2019, and OMB approval for information
provided by test facilities (laboratories and Instrumented Initial Test
Facilities, IITFs) for the National Laboratory Certification Program
(NLCP).
The CCF is used by all Federal agencies and employers regulated by
the Department of Transportation (DOT) and the Nuclear Regulatory
Commission (NRC) to document the collection and chain of custody of
urine specimens at the collection site, for HHS-certified test
facilities to report results, and for Medical Review Officers (MROs) to
document and report a verified result. SAMHSA allows the use of the CCF
as a paper or electronic form.
The current OMB-approved CCF has an August 31, 2020 expiration
date. SAMHSA has resubmitted the CCF with revisions to the form for OMB
approval. During 60-day public comment 7 commenter's submitted comments
on the proposed changes to the CCF. These commenters were comprised of
individuals, organizations, and private sector companies. All comments
were reviewed and taken into consideration in the preparation of the
revised CCF. The issues and concerns raised in the public comments for
the CCF are set out www.reginfo.gov/public/do/PRAMain.
These revisions are listed below:
[[Page 39205]]
Copies 1-5
Revised Step 1
1. Added ``CDL State and No.'' to donor identification types
2. Added ``Collector Contact Info:'' and ``Other'' line (e.g., email)
Revised Step 2
1. Put Urine and Oral Fluid checkboxes above Step 2 for collector to
annotate
2. Expanded to 4 lines for collector entries:
--General entry for Split, Single, or None Provided (same as
current)
--Entries specific to urine collection (moved ``Collector reads
urine temperature within 4 minutes'' here; other entries same as
current)
--Entries specific to oral fluid collection: Added ``Split Type''
with checkboxes for Serial, Concurrent, and Subdivided; ``Each Device
Within Expiration Date?'' with checkboxes Yes or No; and Volume
Indicator(s) Observed checkbox)
--Remarks (same as current)
Revised Step 3
1. Edited instruction to state ``collector affixes seal(s) to
bottle(s)/tube(s)''
Revised Step 4 (Collector Section)
1. Edited ``Specimen Bottle(s) Released To'' box to state ``Specimen
Bottle(s)/Tubes(s) Released To''
Copy 1 (Test Facility Copy)
Revised Step 4 (Accessioner Section)
1. Edited ``Specimen Bottle(s) Released To'' box to state ``Specimen
Bottle(s)/Tubes(s) Released To''
2. Added ``Primary/Single Specimen Device Expiration Date'' and ``Split
Specimen Device Expiration Date'' fields for accessioner to annotate
expiration dates of oral fluid collection devices
Revised Step 5a (Certification and Reporting Section)
1. Removed analyte names and checkboxes
2. Repositioned results and checkboxes: Moved REJECTED FOR TESTING,
ADULTERATED, SUBSTITUTED and INVALID RESULT checkboxes; moved POSITIVE
checkbox to be under DILUTE
3. Added line for certifying scientist to record positive analytes and
concentrations, and added ``Analyte(s) in ng/mL'' instruction (aligned
under ``POSITIVE for:'')
Copy 2 (Medical Review Officer Copy)
Revised Step 5 (Donor Section)
1. Added line for donor email address
2. Edited donor certification statement to state ``specimen bottle/
tubes''
Revised Step 6 (MRO section--Primary Specimen)
1. Put Urine and Oral Fluid checkboxes above Step 6 for MRO to annotate
Bottom of Copies
Revised Copy 1
1. Edited label/seal at bottom of Copy 1 to allow for modification
(e.g., perforations, label with transparent seal on one side, and
separate label and seal)
Revised Copy 5
1. Removed Instructions for Completing the CCF from the back. SAMHSA
will post instructions for completing the Federal CCF for urine and
oral fluid on their website.
Based upon information from Federal agencies and from DOT
concerning their regulated industries, the number of respondents has
increased from 5.4 million to 6.7 million, which increases the total
burden hours by 170,701.8-C;.
Laboratories and IITFs seeking HHS certification under the NLCP
must complete and submit the NLCP application form. The NLCP
application form has not been revised compared to the previous form.
Prior to an inspection, an HHS-certified laboratory or IITF is
required to submit specific information regarding its procedures.
Collecting this information prior to an inspection allows the
inspectors to thoroughly review and understand the testing procedures
before arriving for the onsite inspection. The NLCP information
checklist has not been revised compared to the previous form.
The annual total burden estimates for the CCF, the NLCP
application, the NLCP information checklist, and the NLCP recordkeeping
requirements are shown in the following table.
----------------------------------------------------------------------------------------------------------------
Burden per
Form/respondent Number of Responses per Total number response Annual burden
respondents respondent of responses (hours) (hours)
----------------------------------------------------------------------------------------------------------------
Custody and Control Form: \1\
Donor....................... 6,726,610 1 6,726,610 0.08 538,128.8
Collector................... 6,726,610 1 6,726,610 0.07 378,000
Laboratory.................. 6,726,610 1 6,726,610 0.05 336,330
IITF........................ 1 0 0 0.05 0
Medical Review Officer...... 6,726,610 1 6,726,610 0.05 270,000
NLCP Application Form: \2\
Laboratory.................. 5 5 5 3 15
IITF........................ 0 0 0 3 0
Sections B and C--NLCP
Inspection Checklist:
Laboratory.................. 29 1 29 1 29
IITF........................ 0 0 0 1 0
Record Keeping:
Laboratory.................. 29 1 29 250 7,250
IITF........................ 0 0 0 250 0
-------------------------------------------------------------------------------
Total................... 6,726,673 .............. 26,906,503 .............. 1,529,753
----------------------------------------------------------------------------------------------------------------
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
[[Page 39206]]
for Public Comments'' or by using the search function.
Carlos Graham,
Social Science Analyst.
[FR Doc. 2020-13986 Filed 6-29-20; 8:45 am]
BILLING CODE 4162-20-P
