Mandatory Guidelines for Federal Workplace Drug Testing Programs, 42716-42717 [2016-15469]
Download as PDF
42716
Federal Register / Vol. 81, No. 126 / Thursday, June 30, 2016 / Notices
name and contact information to be
made publicly available, you can
provide this information on the cover
sheet and not in the body of your
comments and you must identify this
information as ‘‘confidential.’’ Any
information marked as ‘‘confidential’’
will not be disclosed except in
accordance with 21 CFR 10.20 and other
applicable disclosure law. For more
information about FDA’s posting of
comments to public dockets, see 80 FR
56469, September 18, 2015, or access
the information at: https://www.fda.gov/
regulatoryinformation/dockets/
default.htm.
Docket: For access to the docket to
read background documents or the
electronic and written/paper comments
received, go to https://
www.regulations.gov and insert the
docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
and/or go to the Division of Dockets
Management, 5630 Fishers Lane, Rm.
1061, Rockville, MD 20852.
Jane
Van Doren, Center for Food Safety and
Applied Nutrition (HFS–005), Food and
Drug Administration, 5100 Campus Dr.,
College Park, MD 20740, 240–402–2927.
FOR FURTHER INFORMATION CONTACT:
In the
Federal Register of April 22, 2016 (81
FR 23733), FDA published a notice
giving interested persons until July 5,
2016, to comment on our request for
scientific data, information, and
comments that would assist us in our
plan to develop a risk assessment for
produce grown in fields or other
growing areas amended with untreated
biological soil amendments of animal
origin (including raw manure).
In early July 2016, the Federal
eRulemaking Portal, https://
www.regulations.gov, is undergoing
maintenance. We are, therefore,
extending the comment period for our
request for scientific data, information,
and comments. The extended comment
period will close on July 19, 2016.
SUPPLEMENTARY INFORMATION:
Dated: June 24, 2016.
Leslie Kux,
Associate Commissioner for Policy.
mstockstill on DSK3G9T082PROD with NOTICES
[FR Doc. 2016–15480 Filed 6–29–16; 8:45 am]
BILLING CODE 4164–01–P
VerDate Sep<11>2014
20:01 Jun 29, 2016
Jkt 238001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
Administration for Children and
Families
Delegation of Authority
Office of the Secretary,
Administration for Children and
Families, HHS.
ACTION: Delegation of authority.
AGENCY:
Notice is hereby given that I
delegate to the Assistant Secretary for
the Administration for Children and
Families (ACF) the following authorities
vested in the Secretary of Health and
Human Services under the Trafficking
Victims Protection Act of 2000 (TVPA),
Public Law 106–386, as amended.
Authority under section
107(b)(1)(B)(i) of the TVPA (22 U.S.C.
7105(b)(1)(B)(i)) to expand benefits and
services to victims of severe forms of
trafficking in persons in the United
States, without regard to immigration
status. In the case of non-entitlement
programs funded by the Secretary of
Health and Human Services, such
benefits and services may include
services to assist potential victims of
trafficking in achieving certification and
to assist minor dependent children of
victims of severe forms of trafficking in
persons or potential victims of
trafficking.
Authority under section
107(b)(1)(B)(ii) of the TVPA (22 U.S.C.
7105(b)(1)(B)(ii)) to make grants for a
national communication system to assist
victims of severe forms of trafficking in
persons in communicating with service
providers.
Authority under section 107(f) of the
TVPA (22 U.S.C. 7105(f)) to establish a
program to assist United States citizens
and aliens lawfully admitted for
permanent residence who are victims of
severe forms of trafficking. In addition
to the authority to provide such victims
with specialized services, the program
also has the authority to identify current
providers and provide a means to make
referrals to programs for which such
victims are already eligible. In the
course of exercising the authority to
conduct activities, personnel in the
Administration for Children and
Families will consult with the Attorney
General, the Secretary of Labor, and
non-governmental organizations that
provide services to victims of severe
forms of trafficking in the United States.
These authorities may be redelegated.
These authorities shall be exercised
under the Department’s policy on
SUMMARY:
PO 00000
Frm 00088
Fmt 4703
Sfmt 4703
regulations and the existing delegation
of authority to approve and issue
regulations.
These delegations shall be exercised
under financial and administrative
requirements applicable to the
Administration for Children and
Families authorities.
I hereby affirm and ratify any actions
taken by the Assistant Secretary for
Children and Families, or your
subordinates, which involved the
exercise of these authorities delegated
herein prior to the effective date of this
delegation.
This delegation supersedes all
existing delegations of these authorities.
DATES: This delegation is effective upon
signature.
Dated: June 21, 2016.
Sylvia M. Burwell,
Secretary.
[FR Doc. 2016–15470 Filed 6–29–16; 8:45 am]
BILLING CODE 4184–34–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Mandatory Guidelines for Federal
Workplace Drug Testing Programs
Substance Abuse and Mental
Health Services Administration
(SAMHSA), Department of Health and
Human Services (HHS).
ACTION: HHS approval of entities that
certify Medical Review Officers (MRO).
AGENCY:
The current version of the
Department of Health and Human
Services (HHS) Mandatory Guidelines
for Federal Workplace Drug Testing
Programs (Mandatory Guidelines),
effective on October 1, 2010, addresses
the role and qualifications of Medical
Review Officers (MROs) and HHS
approval of entities that certify MROs.
DATES: HHS approval is effective June
30, 2016.
FOR FURTHER INFORMATION CONTACT:
Jennifer Fan, Pharm.D., J.D., Division of
Workplace Programs (DWP), Center for
Substance Abuse Prevention (CSAP),
Substance Abuse and Mental Health
Services Administration (SAMHSA),
5600 Fishers Lane, Room 16N02B,
Rockville, MD 20857; Telephone: (240)
276–1759; Email: jennifer.fan@
samhsa.hhs.gov.
SUPPLEMENTARY INFORMATION: Subpart
M-Medical Review Officer (MRO),
section 13.1(b) of the Mandatory
Guidelines, ‘‘Who may serve as an
MRO?’’ states as follows: ‘‘Nationally
recognized entities that certify MROs or
subspecialty boards for physicians
performing a review of Federal
SUMMARY:
E:\FR\FM\30JNN1.SGM
30JNN1
Federal Register / Vol. 81, No. 126 / Thursday, June 30, 2016 / Notices
employee drug testing results that seek
approval by the Secretary must submit
their qualifications and a sample
examination. Based on an annual
objective review of the qualifications
and content of the examination, the
Secretary shall publish a list in the
Federal Register of those entities and
boards that have been approved.’’
HHS has completed its review of
entities that certify MROs, in
accordance with requests submitted by
such entities to HHS.
The HHS Secretary approves the
following MRO certifying entities that
offer MRO certification through
examination:
American Association of Medical
Review Officers (AAMRO), P.O. Box
12873, Research Triangle Park, NC
27709, Phone: (800) 489–1839, Fax:
(919) 490–1010, Email: cferrell@
aamro.com, Web site: https://
www.aamro.com/.
Medical Review Officer Certification
Council (MROCC), 836 Arlington
Heights Road, #327, Elk Grove Village,
IL 60007, Phone: (847) 631–0599, Fax:
(847) 483–1282, Email: mrocc@
mrocc.org, Web site: https://
www.mrocc.org/.
Dated: June 22, 2016.
Sylvia M. Burwell,
Secretary.
[FR Doc. 2016–15469 Filed 6–29–16; 8:45 am]
BILLING CODE P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
mstockstill on DSK3G9T082PROD with NOTICES
Office of the Director; Notice of
Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App), notice is
hereby given of a meeting of the NIH
Clinical Center Research Hospital
Board.
The meeting will be open to the
public as indicated below, with
attendance limited to space available.
Individuals who plan to attend and
need special assistance, such as sign
language interpretation or other
reasonable accommodations, should
notify the Contact Person listed below
in advance of the meeting.
The portions of the meeting devoted
to the identification and evaluation of
specific candidates for consideration for
leadership positions in the Clinical
Center will be closed to the public in
accordance with the provisions set forth
in section 552b(c)(9)(B) and 552b(c)(6),
Title 5 U.S.C., as amended. Premature
VerDate Sep<11>2014
20:01 Jun 29, 2016
Jkt 238001
42717
disclosure of potential candidates and
their qualifications, as well as the
discussions by the committee, could
significantly frustrate NIH’s ability to
recruit these individuals and the
consideration of personnel
qualifications, performance, and the
competence of individuals as candidates
would constitute a clearly unwarranted
invasion of personal privacy.
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: NIH Clinical Center
Research Hospital Board.
Date: July 15, 2016.
Open: 8:30 a.m. to 3:00 p.m.
Agenda: Welcome and NIH Director’s
Overview, Clinical Center Leadership
Feedback, Governance Structure, and Chief
Executive Officer Characteristics.
Place: Conference Room 6C6, Building
31C, National Institutes of Health, Bethesda,
MD 20892.
Closed: 3:15 p.m. to 5:00 p.m.
Agenda: Identification of Candidates for
Leadership Roles.
Place: Conference Room 6C6, Building
31C, National Institutes of Health, Bethesda,
MD 20892.
Contact Person: Gretchen Wood, Staff
Assistant, National Institutes of Health,
Office of the Director, One Center Drive,
Building 1, Room 126, Bethesda, MD 20892,
301–496–4272, woodgs@od.nih.gov.
Any interested person may file written
comments with the committee by forwarding
the statement to the Contact Person listed on
this notice. The statement should include the
name, address, telephone number and when
applicable, the business or professional
affiliation of the interested person.
In the interest of security, NIH has
instituted stringent procedures for entrance
onto the NIH campus. All visitor vehicles,
including taxicabs, hotel, and airport shuttles
will be inspected before being allowed on
campus. Visitors will be asked to show one
form of identification (for example, a
government-issued photo ID, driver’s license,
or passport) and to state the purpose of their
visit.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Topics in
Drug Discovery and Mechanisms of
Antimicrobial Resistance.
Date: July 28–29, 2016.
Time: 8:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: The Westgate Hotel, 1055 Second
Avenue, San Diego, CA 92101.
Contact Person: Guangyong Ji, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 3211,
MSC 7808, Bethesda, MD 20892, 301–435–
1146, jig@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Member
Conflict: Cell Biology, Signaling, and
Development.
Date: July 28, 2016.
Time: 11:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Virtual Meeting).
Contact Person: Thomas Beres, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Dr. Rm. 5201, MSC
7840, Bethesda, MD 20892, 301–435–1175,
berestm@mail.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Member
Conflict: Interdisciplinary Molecular
Sciences.
Date: July 28, 2016.
Time: 1:00 p.m. to 3:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Telephone Conference Call).
Contact Person: Raj K. Krishnaraju, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 6190,
Bethesda, MD 20892, 301–435–1047,
kkrishna@csr.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.306, Comparative Medicine;
93.333, Clinical Research, 93.306, 93.333,
93.337, 93.393–93.396, 93.837–93.844,
93.846–93.878, 93.892, 93.893, National
Institutes of Health, HHS)
Dated: June 24, 2016.
Anna Snouffer,
Deputy Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 2016–15446 Filed 6–29–16; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center For Scientific Review; Notice of
Closed Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meetings.
The meetings will be closed to the
public in accordance with the
provisions set forth in sections
PO 00000
Frm 00089
Fmt 4703
Sfmt 9990
Dated: June 24, 2016.
Anna Snouffer,
Deputy Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 2016–15445 Filed 6–29–16; 8:45 am]
BILLING CODE 4140–01–P
E:\FR\FM\30JNN1.SGM
30JNN1
Agencies
[Federal Register Volume 81, Number 126 (Thursday, June 30, 2016)]
[Notices]
[Pages 42716-42717]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-15469]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Mandatory Guidelines for Federal Workplace Drug Testing Programs
AGENCY: Substance Abuse and Mental Health Services Administration
(SAMHSA), Department of Health and Human Services (HHS).
ACTION: HHS approval of entities that certify Medical Review Officers
(MRO).
-----------------------------------------------------------------------
SUMMARY: The current version of the Department of Health and Human
Services (HHS) Mandatory Guidelines for Federal Workplace Drug Testing
Programs (Mandatory Guidelines), effective on October 1, 2010,
addresses the role and qualifications of Medical Review Officers (MROs)
and HHS approval of entities that certify MROs.
DATES: HHS approval is effective June 30, 2016.
FOR FURTHER INFORMATION CONTACT: Jennifer Fan, Pharm.D., J.D., Division
of Workplace Programs (DWP), Center for Substance Abuse Prevention
(CSAP), Substance Abuse and Mental Health Services Administration
(SAMHSA), 5600 Fishers Lane, Room 16N02B, Rockville, MD 20857;
Telephone: (240) 276-1759; Email: jennifer.fan@samhsa.hhs.gov.
SUPPLEMENTARY INFORMATION: Subpart M-Medical Review Officer (MRO),
section 13.1(b) of the Mandatory Guidelines, ``Who may serve as an
MRO?'' states as follows: ``Nationally recognized entities that certify
MROs or subspecialty boards for physicians performing a review of
Federal
[[Page 42717]]
employee drug testing results that seek approval by the Secretary must
submit their qualifications and a sample examination. Based on an
annual objective review of the qualifications and content of the
examination, the Secretary shall publish a list in the Federal Register
of those entities and boards that have been approved.''
HHS has completed its review of entities that certify MROs, in
accordance with requests submitted by such entities to HHS.
The HHS Secretary approves the following MRO certifying entities
that offer MRO certification through examination:
American Association of Medical Review Officers (AAMRO), P.O. Box
12873, Research Triangle Park, NC 27709, Phone: (800) 489-1839, Fax:
(919) 490-1010, Email: cferrell@aamro.com, Web site: https://www.aamro.com/.
Medical Review Officer Certification Council (MROCC), 836 Arlington
Heights Road, #327, Elk Grove Village, IL 60007, Phone: (847) 631-0599,
Fax: (847) 483-1282, Email: mrocc@mrocc.org, Web site: https://www.mrocc.org/.
Dated: June 22, 2016.
Sylvia M. Burwell,
Secretary.
[FR Doc. 2016-15469 Filed 6-29-16; 8:45 am]
BILLING CODE P