82 FR 30873 - Advisory Committees; Filing of Closed Meeting Reports
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration Federal Register Volume 82, Issue 126 (July 3, 2017)
Food and Drug Administration
Federal Register Volume 82, Issue 126 (July 3, 2017)
| Page Range | 30873-30873 | |
| FR Document | 2017-13886 |
[Federal Register Volume 82, Number 126 (Monday, July 3, 2017)] [Notices] [Page 30873] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2017-13886] ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA-2017-N-0001] Advisory Committees; Filing of Closed Meeting Reports AGENCY: Food and Drug Administration, HHS. ACTION: Notice. ----------------------------------------------------------------------- SUMMARY: The Food and Drug Administration (FDA) is announcing that, as required by the Federal Advisory Committee Act, the Agency has filed with the Library of Congress the annual reports of those FDA advisory committees that held closed meetings during fiscal year 2016. ADDRESSES: Copies are available at the Dockets Management Staff (HFA- 305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852, 240-402-7500. You also may access the docket at https://www.regulations.gov for the annual reports of those FDA advisory committees that held closed meetings during fiscal year 2016. Insert the docket number found in brackets in the heading of this document at https://www.regulations.gov into the ``Search'' box, clear filter under Document Type (left side of screen), and check ``Supporting and Related Material,'' then Sort By Best Match (from the drop-down menu; top right side of screen), ``ID Number (Z-A)'' or Sort By Best Match (from the drop-down menu) ``Title (A-Z),'' also found in the heading of this document. FOR FURTHER INFORMATION CONTACT: Michael Ortwerth, Director and Committee Management Officer, Advisory Committee and Oversight Management Staff, Food and Drug Administration, 10903 New Hampshire Ave., Silver Spring, MD 20993-0002, 301-796-8220. SUPPLEMENTARY INFORMATION: Under section 10(d) of the Federal Advisory Committee Act (5 U.S.C. app.) and 21 CFR 14.60(d), FDA has filed with the Library of Congress the annual reports for the following FDA advisory committees that held closed meetings during the period October 1, 2015, through September 30, 2016: Center for Biologics Evaluation and Research Blood Products Advisory Committee Vaccines and Related Biological Products Advisory Committee National Center for Toxicological Research Science Board to the National Center for Toxicological Research Center for Drugs Evaluation and Research Joint Meetings of the Anesthetic and Analgesic Drug Products Advisory Committee and the Drug Safety and Risk Management Advisory Committee Annual Reports are available for public inspection between 9 a.m. and 4 p.m., Monday through Friday, at: (1) The Library of Congress, Madison Building, Newspaper and Current Periodical Reading Room, 101 Independence Ave. SE., Rm. 133, Washington, DC; and (2) Dockets Management Staff (HFA-305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. Dated: June 27, 2017. Anna K. Abram, Deputy Commissioner for Policy, Planning, Legislation, and Analysis. [FR Doc. 2017-13886 Filed 6-30-17; 8:45 am] BILLING CODE 4164-01-P
![Federal Register / Vol. 82, No. 126 / Monday, July 3, 2017 / Notices 30873
Safety Surveys with the exception of the coverage of U.S. households for in- and Blacks to ensure a minimum of 400
inclusion of addressed based sampling person, mail, telephone, and multimode each. Additionally, methods will be
(ABS) methods to explore the method as surveys (including Web-based surveys.) employed to test for the presence of
a possible alternative for new survey The Food Safety Survey will continue to response bias. Participation in the
questions. ABS is sampling from include cell phones in addition to survey will be voluntary. Cognitive
address frames that are usually based, in landlines for the telephone interviews. interviews and a pre-test will be
part, on residential addresses in the U.S. A nationally representative sample of conducted prior to fielding the survey.
Postal Service Computerized Delivery 4,000 adults will be selected at random
Sequence File. ABS is a cost effective to complete the survey. The survey will FDA estimates the burden of this
method of sampling that provides much also include an oversample of Hispanics collection of information as follows:
TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN 1
Number of Total Average
Number of
Activity responses per annual burden per Total hours
respondents respondent responses response
Cognitive interview screener ............................... 75 1 75 0.083 (5 minutes) ........... 6
Cognitive interview .............................................. 9 1 9 1 ..................................... 9
Pretest screener .................................................. 45 1 45 0.0167 (1 minute) .......... 1
Pretest ................................................................. 18 1 18 0.33 (20 minutes) ........... 6
Survey screener .................................................. 10,000 1 10,000 0.0167 (1 minute) .......... 167
Survey ................................................................. 4,000 1 4,000 0.33 (20 minutes) ........... 1,320
Non-response survey screener ........................... 125 1 125 0.0167 (1 minute) .......... 2
Non-response survey .......................................... 50 1 50 0.167 (10 minutes) ......... 8
Total 2 ........................................................... ........................ ........................ ........................ ........................................ 1,519
1 There are no capital costs or operating and maintenance costs associated with this collection of information.
FDA’s burden estimate is based on the access the docket at https:// National Center for Toxicological
Agency’s prior experience with the www.regulations.gov for the annual Research
Food Safety Survey. FDA estimates that reports of those FDA advisory
the burden hours for this information committees that held closed meetings Science Board to the National Center for
collection will remain the same since during fiscal year 2016. Insert the Toxicological Research
the last OMB approval. docket number found in brackets in the Center for Drugs Evaluation and
Dated: June 27, 2017. heading of this document at https:// Research
Anna K. Abram,
www.regulations.gov into the ‘‘Search’’
box, clear filter under Document Type Joint Meetings of the Anesthetic and
Deputy Commissioner for Policy, Planning,
Legislation, and Analysis.
(left side of screen), and check Analgesic Drug Products Advisory
‘‘Supporting and Related Material,’’ Committee and the Drug Safety and Risk
[FR Doc. 2017–13882 Filed 6–30–17; 8:45 am]
then Sort By Best Match (from the drop- Management Advisory Committee
BILLING CODE 4164–01–P
down menu; top right side of screen),
‘‘ID Number (Z–A)’’ or Sort By Best Annual Reports are available for
Match (from the drop-down menu) public inspection between 9 a.m. and 4
DEPARTMENT OF HEALTH AND p.m., Monday through Friday, at:
HUMAN SERVICES ‘‘Title (A–Z),’’ also found in the heading
of this document. (1) The Library of Congress, Madison
Food and Drug Administration FOR FURTHER INFORMATION CONTACT: Building, Newspaper and Current
Michael Ortwerth, Director and Periodical Reading Room, 101
[Docket No. FDA–2017–N–0001]
Committee Management Officer, Independence Ave. SE., Rm. 133,
Advisory Committees; Filing of Closed Advisory Committee and Oversight Washington, DC; and
Meeting Reports Management Staff, Food and Drug (2) Dockets Management Staff (HFA–
Administration, 10903 New Hampshire 305), Food and Drug Administration,
AGENCY: Food and Drug Administration, Ave., Silver Spring, MD 20993–0002, 5630 Fishers Lane, Rm. 1061, Rockville,
HHS. 301–796–8220.
MD 20852.
ACTION: Notice. SUPPLEMENTARY INFORMATION: Under
section 10(d) of the Federal Advisory Dated: June 27, 2017.
SUMMARY: The Food and Drug Committee Act (5 U.S.C. app.) and 21 Anna K. Abram,
Administration (FDA) is announcing CFR 14.60(d), FDA has filed with the Deputy Commissioner for Policy, Planning,
that, as required by the Federal Library of Congress the annual reports Legislation, and Analysis.
Advisory Committee Act, the Agency for the following FDA advisory [FR Doc. 2017–13886 Filed 6–30–17; 8:45 am]
has filed with the Library of Congress committees that held closed meetings
the annual reports of those FDA BILLING CODE 4164–01–P
sradovich on DSK3GMQ082PROD with NOTICES
during the period October 1, 2015,
advisory committees that held closed through September 30, 2016:
meetings during fiscal year 2016.
ADDRESSES: Copies are available at the Center for Biologics Evaluation and
Dockets Management Staff (HFA–305), Research
Food and Drug Administration, 5630 Blood Products Advisory Committee
Fishers Lane, Rm. 1061, Rockville, MD Vaccines and Related Biological
20852, 240–402–7500. You also may Products Advisory Committee
VerDate Sep<11>2014 17:53 Jun 30, 2017 Jkt 241001 PO 00000 Frm 00058 Fmt 4703 Sfmt 9990 E:\FR\FM\03JYN1.SGM 03JYN1](https://thefederalregister.org/doc/82_FR_30999/page/1.svg)
Document Created: 2018-11-14 10:19:57
Document Modified: 2018-11-14 10:19:57
| Category | Regulatory Information | |
| Collection | Federal Register | |
| sudoc Class | AE 2.7: GS 4.107: AE 2.106: | |
| Publisher | Office of the Federal Register, National Archives and Records Administration | |
| Section | Notices | |
| Action | Notice. | |
| Contact | Michael Ortwerth, Director and Committee Management Officer, Advisory Committee and Oversight Management Staff, Food and Drug Administration, 10903 New Hampshire Ave., Silver Spring, MD 20993-0002, 301-796-8220. | |
| FR Citation | 82 FR 30873 |
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