Agency Information Collection Activities; Proposed Collection; Public Comment Request, 14734-14735 [2017-05627]

Download as PDF 14734 Federal Register / Vol. 82, No. 54 / Wednesday, March 22, 2017 / Notices asabaliauskas on DSK3SPTVN1PROD with NOTICES The Draft EA evaluates the potential environmental impacts that may result from the Proposed Action (referred to as the Build Alternative) and the No Build Alternative on the natural and built environment. Potential impacts of each alternative are evaluated on the following resource categories: Socioeconomics; land use; zoning; public policy; community facilities; transportation; air quality; noise; cultural resources; urban design and visual resources; natural resources; utilities; waste; and greenhouse gases and sustainability. The Draft EA identifies measures to mitigate potential adverse impacts. Availability of the Draft EA: Copies of the Draft EA have been distributed to Federal, State, and local agencies and organizations. The Draft EA is available online in the Federal eRulemaking Portal at www.regulations.gov, identified by Docket No. CDC–2017– 0019. Copies of the Draft EA are also available at: D Chamblee Public Library, 4115 Clairmont Road, Chamblee GA 30341, Telephone: (770) 936–1380. D Doraville Public Library, 3748 Central Ave, Doraville, GA 30340, Telephone: (770) 936–3852. D Brookhaven Branch Public Library, 1242 N. Druid Hills Rd NE., Atlanta, GA 30319, Telephone: (404) 848–7140. D Chamblee City Hall, 5468 Peachtree Road, Chamblee, GA 30341, Telephone: (770) 986–5010. Paper and electronic copies can also be requested as instructed in the ADDRESSES section of this document. Public Meeting: A public meeting will be held on Wednesday, April 19, 2017 at 2400 Century Center, Century Pkwy. NE., Atlanta, Georgia 30345. The public meeting will consist of an Open House from 6:00 p.m. to 8:00 p.m. EDT. The meeting will be an open house where attendees can learn more about the Master Plan and Draft EA, ask questions, and submit comments in writing. Dated: March 15, 2017. Sandra Cashman, Executive Secretary, Centers for Disease Control and Prevention. [FR Doc. 2017–05624 Filed 3–21–17; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2017–N–0001] Food and Drug Administration Center for Drug Evaluation and Research Small Business and Industry Assistance Regulatory Education for Industry Generic Drugs Forum; Public Conference AGENCY: Food and Drug Administration, HHS. ACTION: Notice of public conference. The Food and Drug Administration (FDA) Center for Drug Evaluation and Research (CDER) is sponsoring a 2-day public conference entitled ‘‘FDA CDER Small Business and Industry Assistance (SBIA) Regulatory Education for Industry (REdI) Generic Drugs Forum.’’ The goal of this public conference is to provide direct, relevant, and helpful information on the key aspects of the generic drug development process. Our primary audience is that of small manufacturers within the generic drug industry. However, anyone involved in the pharmaceutical industry may attend. DATES: The public conference will be held April 4–5, 2017, from 8:30 a.m. to 4:30 p.m. See the SUPPLEMENTARY INFORMATION section for registration information. SUMMARY: The public conference will be held in the Pinnacle Ballroom located on the 2nd floor of DoubleTree by Hilton Hotel, 8727 Colesville Rd., Silver Spring, MD 20910. FOR FURTHER INFORMATION CONTACT: Brenda Stodart, Center for Drug Evaluation and Research, Food and Drug Administration, 10001 New Hampshire Ave., Silver Spring, MD 20993–0002, 301–796–6707, email: cdersbia@fda.hhs.gov. SUPPLEMENTARY INFORMATION: ADDRESSES: I. Background FDA is announcing a public conference entitled ‘‘FDA CDER Small Business and Industry Assistance Regulatory Education for Industry Generic Drugs Forum.’’ This public conference is intended to increase the generic drug industry’s awareness of applicable FDA regulations. II. Topics for Discussion at the Public Conference This 2-day, FDA-led forum offers the opportunity to interact with FDA subject matter experts from across CDER involved in the Generic Drug Review VerDate Sep<11>2014 18:14 Mar 21, 2017 Jkt 241001 PO 00000 Frm 00062 Fmt 4703 Sfmt 4703 Program. It will provide up-to-date information on program progress and current initiatives and present a highlevel regulatory overview of the complete ANDA review pathway. III. Participating in the Public Conference Registration: There is no fee to attend the public conference. Space is limited, and registration will be on a first-come, first-served basis. To register, please complete registration online at: https:// www.fda.gov/Drugs/ DevelopmentApprovalProcess/ SmallBusinessAssistance/ ucm540969.htm?utm_ source=FRN&utm_campaign=GDF2017. Early registration is recommended. Registrants will receive email confirmation when they have been accepted, and reminder emails will be sent to registrants 2 days before the conference. If time and space permit, onsite registration will be available beginning at 7:30 a.m. on each day of the public conference. If you need special accommodations due to disability, please contact info@ sbiaevents.com at least 7 days in advance. Streaming Webcast of the Public Conference: This public conference will also be webcast. Persons interested in viewing the webcast must register to receive a confirmation email with the webcast link. If you have never attended a Connect Pro event before, test your connection at https://collaboration.fda.gov/common/ help/en/support/meeting_test.htm. To get a quick overview of the Connect Pro program, visit https://www.adobe.com/ go/connectpro_overview. FDA has verified the Web site addresses in this document, as of the date this document publishes in the Federal Register, but Web sites are subject to change over time. Transcripts: Transcripts will not be available. Dated: March 16, 2017. Leslie Kux, Associate Commissioner for Policy. [FR Doc. 2017–05602 Filed 3–21–17; 8:45 am] BILLING CODE 4164–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Office of the Secretary [Document Identifier: 0955–0009–60D] Agency Information Collection Activities; Proposed Collection; Public Comment Request AGENCY: E:\FR\FM\22MRN1.SGM Office of the Secretary, HHS. 22MRN1 14735 Federal Register / Vol. 82, No. 54 / Wednesday, March 22, 2017 / Notices ACTION: Notice. When submitting comments or requesting information, please include the document identifier 0955–0009–60D for reference. Information Collection Request Title: Customer Relationship Management (CRM) Tool. OMB No.: 0955–0009. Abstract: The Customer Relationship Management (CRM) application is a nimble business intelligence tool being used by more than 1,500 users at ONC partner organizations and grantees. The CRM collects data from a large number of users throughout the United States who are ‘‘on the ground’’ helping healthcare providers adopt and optimize their IT systems, it provides near realtime data about the adoption, utilization, and meaningful use of EHR technology. Approximately half of all Primary Care Providers in the nation are represented in the CRM tool; data points SUPPLEMENTARY INFORMATION: In compliance with the Paperwork Reduction Act of 1995, the Office of the Secretary (OS), Department of Health and Human Services, announces plans to submit an Information Collection Request (ICR), described below, to the Office of Management and Budget (OMB). The ICR is for extending the use of the approved information collection assigned OMB control number 0955– 0009 which expires on May 31, 2017. Prior to submitting the ICR to OMB, OS seeks comments from the public regarding the burden estimate, below, or any other aspect of the ICR. SUMMARY: Comments on the ICR must be received on or before May 22, 2017. DATES: Submit your comments to Information.CollectionClearance@ hhs.gov or by calling (202) 690–5683. ADDRESSES: include provider location, credential, specialty, whether live on an EHR and what system, whether they’ve reached MU, the time between these, and narrative barriers experienced by many of these. Need and Proposed Use of the Information: The CRM tool supplements and is regularly merged with other data sources both within and outside of HHS and tracks program performance and progress towards milestones. Combined with ONC’s internal analytical capacity, this data provides feedback that goes beyond anecdotal evidence and can be turned into tangible lessons learned that are used to focus policy and program efforts and ultimately achieve concrete outcomes. Likely Respondents: HITECH Grantees. The total annual burden hours estimated for this ICR are summarized in the table below. TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS Number of respondents Form name Number of responses per respondent Average burden per response (in hours) Total burden hours CRM Tool—Workforce ...................................................................................................................... CRM Tool—Advance Interoperable HIE Program ............................................................................ CRM Tool—CHP/Academy Health ................................................................................................... 7 24 1 125 24 12 1.5 1.5 1.5 1,313 864 18 Total ........................................................................................................................................... 32 161 4.5 2,195 OS specifically requests comments on (1) the necessity and utility of the proposed information collection for the proper performance of the agency’s functions, (2) the accuracy of the estimated burden, (3) ways to enhance the quality, utility, and clarity of the information to be collected, and (4) the use of automated collection techniques or other forms of information technology to minimize the information collection burden. Terry S. Clark, Asst. Information Collection Clearance Officer. [FR Doc. 2017–05627 Filed 3–21–17; 8:45 am] BILLING CODE 4150–45–P As stipulated by the Federal Advisory Committee Act, the U.S. Department of Health and Human Services (DHHS) is hereby giving notice that a webinar meeting of the Chronic Fatigue Syndrome Advisory Committee (CFSAC) will take place and will be open to the general public to listen in via a toll free number. DATES: The CFSAC webinar will be held on Thursday, June 29, 2017, from 12 p.m. until 5 p.m. (EST) and on Friday, June 30, 2017 from 9 a.m. to 5 p.m. ADDRESSES: This meeting will be broadcasted to the public as a webinar. A webinar is a virtual meeting. Registration is not required for the webinar. SUMMARY: FOR FURTHER INFORMATION CONTACT: asabaliauskas on DSK3SPTVN1PROD with NOTICES DEPARTMENT OF HEALTH AND HUMAN SERVICES Meeting of the Chronic Fatigue Syndrome Advisory Committee Office of the Assistant Secretary for Health, Office of the Secretary, Department of Health and Human Services. AGENCY: ACTION: Notice. VerDate Sep<11>2014 18:14 Mar 21, 2017 Jkt 241001 Gustavo Seinos, MPH, Designated Federal Officer, Chronic Fatigue Syndrome Advisory Committee, Department of Health and Human Services, 200 Independence Avenue SW., Room 728F.6, Washington, DC 20201. Please direct all inquiries to cfsac@hhs.gov. SUPPLEMENTARY INFORMATION: The CFSAC is authorized under 42 U.S.C.217a, Section 222 of the Public Health Service Act, as amended. The PO 00000 Frm 00063 Fmt 4703 Sfmt 4703 purpose of the CFSAC is to provide advice and recommendations to the Secretary of Health and Human Services (HHS), through the Assistant Secretary for Health (ASH), on issues related to myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). The issues can include factors affecting access and care for persons with ME/CFS; the science and definition of ME/CFS; and broader public health, clinical, research, and educational issues related to ME/CFS. The agenda for this meeting, call-in information and location will be posted on the CFSAC Web site https:// www.hhs.gov/ash/advisory-committees/ cfsac/meetings/. A half hour of public comment via telephone will be scheduled for the first half day of the webinar and an entire hour for the second day of the webinar. Individuals will have five minutes to present their comments. Priority will be given to individuals who have not provided public comment within the previous year. We are unable to place international calls for public comments. To request a time slot for public comment, please send an email to cfsac@hhs.gov by June 1, 2017. The email should contain the speaker’s E:\FR\FM\22MRN1.SGM 22MRN1

Agencies

[Federal Register Volume 82, Number 54 (Wednesday, March 22, 2017)]
[Notices]
[Pages 14734-14735]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-05627]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Office of the Secretary

[Document Identifier: 0955-0009-60D]


Agency Information Collection Activities; Proposed Collection; 
Public Comment Request

AGENCY: Office of the Secretary, HHS.

[[Page 14735]]


ACTION: Notice.

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

SUMMARY: In compliance with the Paperwork Reduction Act of 1995, the 
Office of the Secretary (OS), Department of Health and Human Services, 
announces plans to submit an Information Collection Request (ICR), 
described below, to the Office of Management and Budget (OMB). The ICR 
is for extending the use of the approved information collection 
assigned OMB control number 0955-0009 which expires on May 31, 2017. 
Prior to submitting the ICR to OMB, OS seeks comments from the public 
regarding the burden estimate, below, or any other aspect of the ICR.

DATES: Comments on the ICR must be received on or before May 22, 2017.

ADDRESSES: Submit your comments to 
Information.CollectionClearance@hhs.gov or by calling (202) 690-5683.

SUPPLEMENTARY INFORMATION: When submitting comments or requesting 
information, please include the document identifier 0955-0009-60D for 
reference.
    Information Collection Request Title: Customer Relationship 
Management (CRM) Tool.
    OMB No.: 0955-0009.
    Abstract: The Customer Relationship Management (CRM) application is 
a nimble business intelligence tool being used by more than 1,500 users 
at ONC partner organizations and grantees. The CRM collects data from a 
large number of users throughout the United States who are ``on the 
ground'' helping healthcare providers adopt and optimize their IT 
systems, it provides near real-time data about the adoption, 
utilization, and meaningful use of EHR technology. Approximately half 
of all Primary Care Providers in the nation are represented in the CRM 
tool; data points include provider location, credential, specialty, 
whether live on an EHR and what system, whether they've reached MU, the 
time between these, and narrative barriers experienced by many of 
these.
    Need and Proposed Use of the Information: The CRM tool supplements 
and is regularly merged with other data sources both within and outside 
of HHS and tracks program performance and progress towards milestones. 
Combined with ONC's internal analytical capacity, this data provides 
feedback that goes beyond anecdotal evidence and can be turned into 
tangible lessons learned that are used to focus policy and program 
efforts and ultimately achieve concrete outcomes.
    Likely Respondents: HITECH Grantees.
    The total annual burden hours estimated for this ICR are summarized 
in the table below.

                                    Total Estimated Annualized Burden--Hours
----------------------------------------------------------------------------------------------------------------
                                                                     Number of    Average burden
                    Form name                        Number of     responses per   per response    Total burden
                                                    respondents     respondent      (in hours)         hours
----------------------------------------------------------------------------------------------------------------
CRM Tool--Workforce.............................               7             125             1.5           1,313
CRM Tool--Advance Interoperable HIE Program.....              24              24             1.5             864
CRM Tool--CHP/Academy Health....................               1              12             1.5              18
                                                 ---------------------------------------------------------------
    Total.......................................              32             161             4.5           2,195
----------------------------------------------------------------------------------------------------------------

    OS specifically requests comments on (1) the necessity and utility 
of the proposed information collection for the proper performance of 
the agency's functions, (2) the accuracy of the estimated burden, (3) 
ways to enhance the quality, utility, and clarity of the information to 
be collected, and (4) the use of automated collection techniques or 
other forms of information technology to minimize the information 
collection burden.

Terry S. Clark,
Asst. Information Collection Clearance Officer.
[FR Doc. 2017-05627 Filed 3-21-17; 8:45 am]
 BILLING CODE 4150-45-P
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.