Proposed Data Collection Submitted for Public Comment and Recommendations
| Published date | 08 September 2020 |
| Citation | 85 FR 55454 |
| Record Number | 2020-19746 |
| Section | Notices |
| Court | Agency For Toxic Substances And Disease Registry,Health And Human Services Department |
55454
Federal Register / Vol. 85, No. 174 / Tuesday, September 8, 2020 / Notices
performance characteristics of the
broadband connection and the kind of
handsets and versions of operating
systems tested. Information the FCC
Speed Test App (‘‘Application’’) collects
is limited to information used to
measure volunteers’ mobile broadband
service and no personally identifiable
information, such as subscribers’ name,
phone number or unique identifiers
associated with a device is collected.
Software-based tools and online tools
exist that can test consumer’s broadband
connections, including a set of
consumer tools launched by the FCC in
conjunction with the National
Broadband Plan. However, these tools
track speeds experienced by consumers,
rather than speeds delivered directly to
a consumer by an ISP. The distinction
is important for supporting Agency
broadband policy analysis, as ISPs
advertise speeds and performance
delivered rather than speeds
experienced, which suffers from
degradation outside of an ISP’s control.
No other dedicated panel of direct
fixed and mobile broadband
performance measurement using
publicly documented methodologies
using free and add-free technologies
exists today in the country. The program
will continue to support existing
software-based tools and online tools
but the focus of the program will remain
the direct measurement of broadband
performance delivered to the consumer.
The collection effort also has specific
elements focused on further network
performance statistics, time of day
parameters, and other elements affecting
consumers’ broadband experience that
are not tracked elsewhere. The
information to be confirmed by ISP
Partners about their subscribers or
technical and market data regarding the
broadband services they provide is
unavailable from other sources.
Federal Communications Commission.
Marlene Dortch,
Secretary, Office of the Secretary.
[FR Doc. 2020–19684 Filed 9–4–20; 8:45 am]
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[FR Doc. 2020–19780 Filed 9–4–20; 8:45 am]
BILLING CODE P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Toxic Substances and
Disease Registry
[60Day–20–0051; Docket No. ATSDR–2020–
0005]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
AGENCY
: Agency for Toxic Substances
and Disease Registry (ATSDR),
Department of Health and Human
Services (HHS).
ACTION
: Notice with comment period.
SUMMARY
: The Agency for Toxic
Substances and Disease Registry
(ATSDR), as part of its continuing effort
to reduce public burden and maximize
the utility of government information,
invites the general public and other
Federal agencies the opportunity to
comment on a proposed and/or
continuing information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection project titled ‘‘Assessment of
Chemical Exposures (ACE)
Investigations.’’ The purpose of ACE
Investigations is to focus on performing
rapid epidemiological assessments to
assist state, regional, local, or tribal
health departments (the requesting
agencies) to respond to or prepare for
acute environmental incidents.
DATES
: ATSDR must receive written
comments on or before November 9,
2020.
ADDRESSES
: You may submit comments,
identified by Docket No. ATSDR–2020–
0005 by any of the following methods:
•Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
•Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE, MS–D74, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. ATSDR will post,
without change, all relevant comments
to Regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT
: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS–
D74, Atlanta, Georgia 30329; phone:
404–639–7118; Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION
: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. 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;
2. 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;
3. Enhance the quality, utility, and
clarity of the information to be
collected; and
4. Minimize the burden of the
collection of information on those who
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55455
Federal Register / Vol. 85, No. 174 / Tuesday, September 8, 2020 / Notices
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 submissions
of responses.
5. Assess information collection costs.
Proposed Project
Assessment of Chemical Exposures
(ACE) Investigations (OMB Control No.
0923–0051, Exp. 03/31/2021)—Revision
—Agency for Toxic Substances and
Disease Registry (ATSDR).
Background and Brief Description
The Agency for Toxic Substances and
Disease Registry (ATSDR) is requesting
a three-year Paperwork Reduction Act
(PRA) clearance for the Revision of
‘‘Assessment of Chemical Exposures
(ACE) Investigations’’ information
collection request (ICR)(OMB Control
No. 0923–0051; Expiration Date 03/31/
2021). ATSDR conducts ACE
Investigations to assist state and local
health departments after acute
environmental incidents.
ATSDR has successfully completed
five investigations to date using this
valuable mechanism. ATSDR would like
to continue these impactful information
collections. A brief summary of recent
information collections approved under
this tool includes the following:
•During 2015, in U.S. Virgin Islands
there was a methyl bromide exposure
incident at a condominium resort
severely injuring a family and causing
symptoms in the first responders to the
incident. ATSDR interviewed all
potentially exposed persons who stayed
or worked at the resort to look for signs
of exposure. Under this ACE
investigation, ATSDR raised awareness
among pest control companies that
methyl bromide is currently prohibited
in homes and other residential settings.
Additionally, ATSDR raised awareness
among clinicians about the toxicologic
syndrome caused by exposure to methyl
bromide and the importance of notifying
first responders immediately when they
have encountered contaminated
patients.
•During 2016, the ACE Team
conducted a rash investigation in Flint,
Michigan. Persons who were exposed to
Flint municipal water and had current
or worsening rashes were surveyed and
referred to free dermatologist screening
if desired. Findings revealed that when
the city was using water from the Flint
River, there were large swings in
chorine, pH, and hardness, which could
be one possible explanation for the
eczema-related rashes.
•During 2016, the ACE Team also
conducted a follow-up investigation for
people who were referred to a
dermatologist in the first Flint
investigation. The follow-up interviews
resulted in improvements in medical
exam and referral processes that were
still on-going at the time.
The ACE Investigations have focused
on performing rapid epidemiological
assessments to assist state, regional,
local, or tribal health departments (the
requesting agencies) to respond to or
prepare for acute chemical releases.
The main objectives for performing
these rapid assessments are to:
•Characterize exposure and acute
health effects of the affected community
to inform health officials and the
community;
•Identify needs (i.e., medical, mental
health, and basic) of those exposed
during the incidents to aid in planning
interventions in the community;
•Determine the sequence of events
responsible for the incident so that
actions can be taken to prevent future
incidents;
•Assess the impact of the incidents
on the emergency response and health
services use and share lessons learned
for use in hospital, local, and state
planning for environmental incidents;
and
•Identify cohorts that may be
followed and assessed for persistent
health effects resulting from
environmental releases.
Because each incident is different, it
is not possible to predict in advance
exactly what type of, and how many
respondents will be consented and
interviewed to effectively evaluate the
incident. Respondents typically include,
but are not limited to, emergency
responders such as police, fire,
hazardous material technicians,
emergency medical services, and
personnel at hospitals where patients
from the incident were treated.
Incidents may occur at businesses or in
the community setting; therefore,
respondents may also include business
owners, managers, workers, customers,
community residents, and those passing
through the affected area.
The multidisciplinary ACE Team
consisting of staff from ATSDR, the
Centers for Disease Control and
Prevention (CDC), and the requesting
agencies will be collecting data. ATSDR
has developed a quickly tailored series
of draft survey forms used in the field
to collect data that will meet the goals
of the investigation. ATSDR collections
will be administered based on time
permitted and urgency. For example, it
is preferable to administer the General
Survey to as many respondents as
possible. However, if there are time
constraints, the shorter Household
Survey or the former ACE Short Form,
now modified as the Epidemiologic
Contact Assessment Symptom Exposure
(Epi CASE) Survey, may be
administered instead. The individual
surveys collect information about
exposure, acute health effects, health
services use, medical history, needs
resulting from the incident,
communication during the release,
health impact on children, and
demographic data. Hospital personnel
are asked about the surge, response and
communication, decontamination, and
lessons learned.
Depending on the situation, data
collected by face-to-face interviews,
telephone interviews, written surveys,
mailed surveys, or on-line surveys can
be collected. Medical charts may also be
considered for review. In rare situations,
an investigation might involve
collection of clinical specimens.
ATSDR is proposing to increase the
utility of this Generic ICR in response to
stakeholder requests. We would like to
expand the ACE toolkit to be more
inclusive of other types of
environmental incidents affecting the
community and which fall under
ATSDR’s mandate and, at times, the
mandates of our partners in the CDC’s
National Center for Environmental
Health (NCEH) and the National Center
for Occupational Safety and Health
(NIOSH). In addition to acute chemical
releases, we propose to include
radiological and nuclear incidents,
explosions, natural disasters, and other
environmental incidents.
We propose revisions to select
information collection forms, which
will be deployed using handheld
devices whenever possible to reduce
burden, and to adjust the number of
responses and time per response for
several forms. A new brief Eligibility
Screener (900 responses per year; 30
hours) will be added prior to
administering consent for our surveys.
The Epi CASE Survey, formerly the ACE
Short Form, has been modified for the
expanded scope of eligible incidents
requested (1,000 responses per year; 250
hours). To reduce time burden, there
will be new field data entry screens and
deletion of unused questions for the
General Survey (800 responses per year;
333 hours), the Household Survey (120
responses per year; 20 hours) and for the
Hospital Survey (40 responses per year;
17 hours). We are retaining the Medical
Chart Abstraction Form (250 responses
per year; 125 hours) but are removing
the Veterinary Chart Abstraction Form
as it has not been used in the past.
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Federal Register / Vol. 85, No. 174 / Tuesday, September 8, 2020 / Notices
ATSDR anticipates up to four ACE
investigations per year. We are
requesting approval for 3,110 annual
responses (increase of 1,820 responses
per year) and for 775 annual hours
(increase of 184 hours per year).
Participation in ACE investigations is
voluntary and there are no anticipated
costs to respondents other than their
time.
E
STIMATED
A
NNUALIZED
B
URDEN
H
OURS
Type of
respondent Form name Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hr)
Total
burden
(in hr)
Residents, first responders, business owners, employees,
customers ......................................................................... Eligibility
Screener 900 1 2/60 30
Epi CASE
Survey 1,000 1 15/60 250
General
Survey 800 1 25/60 333
Residents ............................................................................. Household
Survey 120 1 10/60 20
Hospital staff ........................................................................ Hospital
Survey 40 1 25/60 17
Staff from state, local, or tribal health agencies .................. Medical Chart
Abstraction
Form
25 10 30/60 125
Total .............................................................................. ........................ ........................ ........................ ........................ 775
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2020–19746 Filed 9–4–20; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–20–20EC]
Agency Forms Undergoing Paperwork
Reduction Act Review
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled Enterprise
Laboratory Information Management
System (ELIMS) to the Office of
Management and Budget (OMB) for
review and approval. CDC previously
published a ‘‘Proposed Data Collection
Submitted for Public Comment and
Recommendations’’ notice on December
23, 2019 to obtain comments from the
public and affected agencies. CDC
received one comment related to the
previous notice. This notice serves to
allow an additional 30 days for public
and affected agency comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(a) 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;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) 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; and
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570.
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. Direct written
comments and/or suggestions regarding
the items contained in this notice to the
Attention: CDC Desk Officer, Office of
Management and Budget, 725 17th
Street NW, Washington, DC 20503 or by
fax to (202) 395–5806. Provide written
comments within 30 days of notice
publication.
Proposed Project
Enterprise Laboratory Information
Management System (ELIMS) Existing
Collection in Use without an OMB
control number—National Center for
Emerging and Zoonotic Infectious
Diseases (NCEZID), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
The collection of specimen
information designated for testing by the
CDC occurs on a regular and recurring
basis (multiple times per day) using an
electronic PDF file called the CDC
Specimen Submission 50.34 Form or an
electronic XSLX file called the Global
File Accessioning Template. Hospitals,
doctor’s offices, medical clinics,
commercial testing labs, universities,
state public health laboratories, U.S.
federal institutions and foreign
institutions use the CDC Specimen
Submission Form 50.34 when
submitting a single specimen to CDC
Infectious Diseases laboratories for
testing. The CDC Specimen Submission
50.34 Form consists of over 200 data
entry fields (of which five are
mandatory fields that must be
completed by the submitter) that
captures information about the
specimen being sent to the CDC for
testing. The type of data captured on the
50.34 Form identifies the origin of the
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