Statement of Organization, Functions, and Delegations of Authority, 70423-70425 [2016-24640]
Download as PDF
Federal Register / Vol. 81, No. 197 / Wednesday, October 12, 2016 / Notices
C. Public Comments
Public comments are particularly
invited on: Whether this collection of
information is necessary for the proper
performance of functions of the FAR,
and whether it will have practical
utility; whether our estimate of the
public burden of this collection of
information is accurate, and based on
valid assumptions and methodology;
ways to enhance the quality, utility, and
clarity of the information to be
collected; and ways in which we can
minimize the burden of the collection of
information on those who are to
respond, through the use of appropriate
technological collection techniques or
other forms of information technology.
Obtaining Copies of Proposals:
Requesters may obtain a copy of the
information collection documents from
the General Services Administration,
Regulatory Secretariat Division (MVCB),
1800 F Street NW., Washington, DC
20405, telephone 202–501–4755. Please
cite OMB Control No. 9000–0138,
Contract Financing, in all
correspondence.
Dated: October 5, 2016.
Lorin S. Curit,
Director, Federal Acquisition Policy Division,
Office of Governmentwide Acquisition Policy,
Office of Acquisition Policy, Office of
Governmentwide Policy.
[FR Doc. 2016–24538 Filed 10–11–16; 8:45 am]
BILLING CODE 6820–EP–P
DEPARTMENT OF DEFENSE
GENERAL SERVICES
ADMINISTRATION
NATIONAL AERONAUTICS AND
SPACE ADMINISTRATION
[OMB Control No. 9000–0096; Docket No.
2016–0053; Sequence No. 31]
Submission for OMB Review; Patents
Department of Defense (DOD),
General Services Administration (GSA),
and National Aeronautics and Space
Administration (NASA).
ACTION: Notice of request for comments
regarding an extension to an existing
OMB clearance.
AGENCY:
Under the provisions of the
Paperwork Reduction Act, the
Regulatory Secretariat Division will be
submitting to the Office of Management
and Budget (OMB) a request to review
and approve an extension of a
previously approved information
collection requirement concerning
patents. A notice was published in the
Federal Register at 81 FR 43607 on July
5, 2016. No comments were received.
mstockstill on DSK3G9T082PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
20:13 Oct 11, 2016
Jkt 241001
Submit comments on or before
November 14, 2016.
ADDRESSES: Submit comments regarding
this burden estimate or any other aspect
of this collection of information,
including suggestions for reducing this
burden to: Office of Information and
Regulatory Affairs of OMB, Attention:
Desk Officer for GSA, Room 10236,
NEOB, Washington, DC 20503.
Additionally submit a copy to GSA by
any of the following methods:
• Regulations.gov: https://
www.regulations.gov. Submit comments
via the Federal eRulemaking portal by
searching for ‘‘9000–0096; Patents’’.
Select the link ‘‘Submit a Comment’’
that corresponds with ‘‘Information
Collection 9000–0096, Patents’’. Follow
the instructions provided at the ‘‘Submit
a Comment’’ screen. Please include your
name, company name (if any), and
‘‘Information Collection 9000–0096,
Patents’’ on your attached document.
• Mail: General Services
Administration, Regulatory Secretariat
Division (MVCB), IC 9000–0096, 1800 F
Street NW., Washington, DC 20405.
Instructions: Please submit comments
only and cite Information Collection
9000–0096, Patents, in all
correspondence related to this
collection. Comments received generally
will be posted without change to https://
www.regulations.gov, including any
personal and/or business confidential
information provided. To confirm
receipt of your comment(s), please
check www.regulations.gov,
approximately two to three days after
submission to verify posting (except
allow 30 days for posting of comments
submitted by mail).
FOR FURTHER INFORMATION CONTACT: Mr.
Charles Gray, Procurement Analyst,
Federal Acquisition Policy Division, at
703–795–6328 or email charles.gray@
gsa.gov.
SUPPLEMENTARY INFORMATION:
DATES:
A. Purpose
The patent coverage in Federal
Acquisition Regulation (FAR) subpart
27.2 requires the contractor to report
each notice of a claim of patent or
copyright infringement that came to the
contractor’s attention in connection
with performing a Government contract
(FAR 27.202–1 and 52.227–2).
The contractor is also required to
report all royalties anticipated or paid in
excess of $250 for the use of patented
inventions by furnishing the name and
address of licensor, date of license
agreement, patent number, brief
description of item or component,
percentage or dollar rate of royalty per
unit, unit price of contract item, and
PO 00000
Frm 00038
Fmt 4703
Sfmt 4703
70423
number of units (FAR 27.202–5, 52.227–
6, and 52.227–9).
B. Annual Reporting Burden
Number of Respondents: 107.
Responses per Respondent: 1.
Total Annual Responses: 107.
Hours per Response: 1.17.
Estimated Total Burden Hours: 126.
Frequency: On Occasion.
Affected Public: Businesses or otherfor-profit entities and not-for-profit
institutions.
C. Public Comments
Public comments are particularly
invited on: Whether this collection of
information is necessary for the proper
performance of functions of the FAR,
and whether it will have practical
utility; whether our estimate of the
public burden of this collection of
information is accurate, and based on
valid assumptions and methodology;
ways to enhance the quality, utility, and
clarity of the information to be
collected; and ways in which we can
minimize the burden of the collection of
information on those who are to
respond, through the use of appropriate
technological collection techniques or
other forms of information technology.
Obtaining Copies of Proposals:
Requesters may obtain a copy of the
information collection documents from
the General Services Administration,
Regulatory Secretariat Division (MVCB),
1800 F Street NW., Washington, DC
20405, telephone 202–501–4755.
Please cite OMB Control No. 9000–
0096, Patents, in all correspondence.
Dated: October 5, 2016.
Lorin S. Curit,
Director, Federal Acquisition Policy Division,
Office of Governmentwide Acquisition Policy,
Office of Acquisition Policy, Office of
Governmentwide Policy.
[FR Doc. 2016–24537 Filed 10–11–16; 8:45 am]
BILLING CODE 6820–14–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Statement of Organization, Functions,
and Delegations of Authority
Part C (Centers for Disease Control
and Prevention) of the Statement of
Organization, Functions, and
Delegations of Authority of the
Department of Health and Human
Services (45 FR 67772–76, dated
October 14, 1980, and corrected at 45 FR
69296, October 20, 1980, as amended
most recently at 81 FR 66284–66285,
E:\FR\FM\12OCN1.SGM
12OCN1
mstockstill on DSK3G9T082PROD with NOTICES
70424
Federal Register / Vol. 81, No. 197 / Wednesday, October 12, 2016 / Notices
dated September 27, 2016) is amended
to reflect the reorganization of the
Division of Scientific Resources,
National Center for Emerging and
Zoonotic Infectious Diseases, Office of
Infectious Diseases, Centers for Disease
Control and Prevention.
Section C–B, Organization and
Functions, is hereby amended as
follows:
Delete and replace the title and the
mission and function statements for the
Division of Scientific Resources (CVLH)
and insert the following:
Division of Scientific Resources
(CVLH). The Division of Scientific
Resources (DSR) provides products,
services, and specialized expertise to
CDC staff and activities in support of
research and service activities: In
carrying out its mission, DSR: (1)
Provides animals, laboratory supplies,
animal and human blood products,
glassware, mammalian tissue cultures,
microbiological media, special reagents,
and other laboratory materials in
support of research and service
activities to laboratories and
investigators at CDC; (2) develops and
implements applied research programs
to expand and enhance the use of
animal models necessary to support
research and diagnostic programs and to
improve breeding and husbandry
procedures; (3) conducts applied
research in cell biology and in the
expansion of tissue culture technology
as a research and diagnostic tool for
infectious disease activities; (4) provides
services for laboratory investigators in
protein and DNA synthesis and
sequencing, genomic sequencing,
microarrays, proteomics, and molecular
modeling; (5) maintains a bank of serum
and other biological specimens of
epidemiological and special significance
to CDC’s research and diagnostic
activities; (6) obtains and distributes
experimental and orphaned vaccines,
drugs, antisera, antitoxins, and immune
globulins; (7) manages and distributes
the inventory, maintains the
computerized system database, and
provides general technical service
support for the dispensing, lyophilizing,
capping, and labeling of CDC reference
reagents; (8) receives, triages, processes,
and distributes specimens to CDC
laboratories for reference diagnostic
testing, research studies, and epidemics
and reports diagnostic test results to
submitting organizations; (9) manages
all CDC exports and ensures compliance
with regulations and serves as CDC
liaison with the Department of
Commerce for export related issues; (10)
produces and distributes specialized
reagents and kits for the detection of
select agents to members of the
VerDate Sep<11>2014
20:13 Oct 11, 2016
Jkt 241001
Laboratory Response Network; (11)
provides services and expertise in
development of quality systems to
support compliance with the Food and
Drug Administration regulations on
production, distribution, and use of
laboratory diagnostic reagents; (12)
provides liaison activities, resources,
and expertise for inquiries related to
animals and zoonotic diseases; and (13)
provides a centralized activity for
tracking requests for and distributing
select agents to investigators outside of
CDC in compliance with federal
regulations.
Office of the Director (CVLH1). (1)
Manages, directs, and coordinates the
activities of DSR; (2) provides
leadership and guidance on policy,
budget, program planning and
development, program management,
and operations; (3) provides DSR-wide
administrative and program services
and coordinates or ensures coordination
with the appropriate CIOs, OID, and
CDC staff offices on administrative and
program matters; (4) provides liaison
with other governmental agencies,
international organizations, and other
outside groups; (5) coordinates, in
collaboration with the appropriate CIOs,
OID, and CDC components, laboratory
activities relating to support of outbreak
investigations or laboratory-based
research including but not limited to
specimen management, biological
reagents, and laboratory supplies; (6)
maintains a formulary of investigational
and licensed drugs and biologicals that
are distributed to approved physicians
for the prevention, control, and/or
treatment of rare, tropical, or
exceptional diseases; (7) advises the
Director, NCEZID, on policy matters
concerning DSR activities; and (8)
coordinates technical services for
laboratory activities of CDC programs
including procurement of glassware and
laboratory supplies.
Comparative Medicine Branch
(CVLHB). (1) Acquires and distributes
laboratory animals for research; (2)
provides appropriate housing,
husbandry, and psychological
enrichment for all research animals; (3)
provides veterinary services, including
clinical and surgical support, for the
laboratory animals; (4) develops
standard operating procedures for
animal care and use in accordance with
the policies established by the American
Association for Accreditation of
Laboratory Animal Care, the Animal
Welfare Act, The Guide for the Care &
Use of Laboratory Animals, and the CDC
International Animal Care & Use
Committee; (5) conducts applied
research to improve the care and use of
animals in research and collaborates on
PO 00000
Frm 00039
Fmt 4703
Sfmt 4703
research projects that use laboratory
animals; (6) provides consultation and
laboratory animal technology training to
investigators, technical staff and animal
care personnel; (7) provides oversight,
support and investigator training for the
graphical animal information
technology protocol development and
animal tracking database; (8)
coordinates technical services for
laboratory activities of CDC programs
including processing and distribution of
glassware and related items, laboratory
waste decontamination and disposal,
laundry services, and materiel
management; and (9) provides autoclave
label production services.
Biotechnology Core Facility Branch
(CVLHD). (1) provides state-of-the-art
next-generation genomic sequencing
and metagenomics analysis of infectious
and biothreat agents; (2) provides
optical mapping to produce high
resolution whole-genome maps for
strain typing, molecular epidemiology,
comparative genomics, and quality
control for whole genome sequence
assembly; (3) provides computational
analysis of genomics sequencing data,
bioinformatics, and biological
computing; (4) provides qualitative and
quantitative proteomic analyses
(identification of expressed proteins by
mass spectrometry); analysis of
functionally-relevant post-translational
modifications of proteins; (5) provides
mass spectrometry-based positive
identification of bacteria and fungi
(BioTyperTM, Bruker Daltonics); (6)
provides synthetic oligonucleotide
chemistry in support of development of
rapid diagnostic tests and
characterization of pathogens and their
hosts; (7) provides synthetic peptide
chemistry in support of studies of
immune response and antigen-antibody
interactions; (8) provides biotechnology
seminars and methods evaluation; (9)
provides laboratory equipment design
and repair services to all CDC; and (10)
collaborates on research related to STD
transmitted infections as chronic
infectious diseases.
Reagent and Diagnostic Services
Branch (CVLHG). (1) maintains
laboratory water treatment systems to
ensure quality of CDC reagent grade
laboratory water; (2) produces,
develops, evaluates and distributes
custom microbiological and cell culture
media, buffers and chemical reagent,
mammalian and insect cell cultures,
hybridomas, monoclonal and
polycolonal antibodies, and in vitro
diagnostic products for diagnostic
research purposes, proficiency testing,
pandemic preparedness, outbreak
response and surveillance activities; (3)
collaborates with subject matter experts
E:\FR\FM\12OCN1.SGM
12OCN1
70425
Federal Register / Vol. 81, No. 197 / Wednesday, October 12, 2016 / Notices
in regulatory compliant development,
production, packaging, storing and
distribution of BSL2/BSL3 reagents,
select agents, novel immuno-chemical
reagents and reference diagnostic
reagents; (4) provides dispensing,
lyophilizing, label production, and
device assembly services; (5) improves
the process of bench-top development
and in-house pilot scale production
providing immediate availability for
distribution, preventing backorders and
streamlining commercialization; (6)
maintains CDC’s Biological Reference
Reagent Inventory, mammalian cell line
repository and a serviceable inventory at
the DSR Continuity of Operations
storage facility; (7) provides centralized
specimen management services for
diagnostic, reference, and outbreak
investigations; maintains a bank of
biological specimens of epidemiological
significance to CDC’s research and
diagnostic activities; manages and tracks
systems of specimen collections; (8)
receives, triages, processes, stores and
distributes specimens to CDC
laboratories for reference diagnostic
testing, research studies, and reports
diagnostic and surveillance test results
to submitting organizations; (9) serves as
central facility for acquisition and
distribution of fresh human blood,
blood products, and serum in bulk; (10)
packages and ships infectious
substances and other materials, ensuring
compliance with regulations for
shipping clinical specimens, infectious
substances, and other materials; (11)
manages all CDC exports and ensures
compliance with regulations and serves
as CDC liaison with Department of
Commerce for export related issues; and
(12) provides consultation in all of the
above technical services.
Sherri Berger,
Chief Operating Officer, Centers for Disease
Control and Prevention.
[FR Doc. 2016–24640 Filed 10–11–16; 8:45 am]
BILLING CODE 4160–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Agency Recordkeeping/Reporting
Requirements Under Emergency
Review by the Office of Management
and Budget (OMB)
Title: Provision of Child Support
Services in IV–D cases under the Hague
Child Support Convention; Federally
Approved Forms.
OMB No.: New Collection.
Description: On January 1, 2017, the
2007 Hague Convention on the
International Recovery of Child Support
and Other Forms of Family Maintenance
will enter into force for the United
States. This Convention contains
groundbreaking provisions that, for the
first time on a worldwide scale, will
establish uniform, simple, fast, and
inexpensive procedures for the
processing of international child
support cases. Once the Convention is
in effect, U.S. states will process child
support cases with other countries that
have ratified the Convention under the
requirements of the Convention and
article 7 of the Uniform Interstate
Family Support Act (UIFSA 2008). In
order to comply with the Convention,
the U.S. must implement the
Convention’s case processing forms.
State and Federal law require states to
use federally-approved case processing
forms. Section 311(b) of UIFSA 2008,
which has been enacted by all 50 states,
the District of Columbia, Guam, Puerto
Rico and the Virgin Islands, requires
States to use forms mandated by Federal
law. 45 CFR 303.7 also requires child
support programs to use federallyapproved forms in intergovernmental
IV–D cases unless a country has
provided alternative forms as a part of
its chapter in a Caseworker’s Guide to
Processing Cases with Foreign
Reciprocating Countries.
Respondents: State agencies
administering a child support program
under title IV–D of the Social Security
Act.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
mstockstill on DSK3G9T082PROD with NOTICES
Annex I: Transmittal form under Article 12(2) .................................................
Annex II: Acknowledgment form under Article 12(3) .......................................
Annex A: Application for Recognition and Enforcement, including restricted
information on the applicant .........................................................................
Annex A: Abstract of Decision .........................................................................
Annex A: Statement of Enforceability of Decision ...........................................
Annex A: Statement of Proper Notice .............................................................
Annex A: Status of Application Report ............................................................
Annex B: Application for Enforcement of a Decision Made or Recognized in
the Requested State, including restricted information on the applicant ......
Annex B: Status of Application Report, Article 12 ...........................................
Annex C: Application for Establishment of a Decision, including restricted
information on the Applicant ........................................................................
Annex C: Status of Application Report—Article 12 .........................................
Annex D: Application for Modification of a Decision, including Restricted Information on the Applicant ...........................................................................
Annex D: Status of Application Report—Article 12 .........................................
Annex E: Financial Circumstances Form ........................................................
Estimated Total Annual Burden
Hours: 13,478.
Additional Information: ACF is
requesting that OMB grant a 180 day
approval for this information collection
under procedures for emergency
processing by October 20, 2016. A copy
VerDate Sep<11>2014
20:13 Oct 11, 2016
Jkt 241001
Frm 00040
Fmt 4703
Sfmt 4703
Average
burden hours
per response
Total burden
hours
54
54
46
93
1
.5
2,484
2,511
54
54
54
54
54
19
5
19
5
37
.5
1
0.17
.5
.33
513
270
174
135
659
54
54
19
37
.5
.33
513
659
54
54
5
9
.5
.33
135
160
54
54
54
5
9
46
.5
.33
2
135
160
4,968
of this information collection, with
applicable supporting documentation,
may be obtained by calling the
Administration for Children and
Families, Reports Clearance Officer,
Robert Sargis at (202) 690–7275.
PO 00000
Number of
responses per
respondent
Comments and questions about the
information collection described above
should be directed to the Office of
Information and Regulatory Affairs,
Attn: OMB Desk Officer for ACF, Office
of Management and Budget, Paperwork
Reduction Project, 725 17th Street NW.,
E:\FR\FM\12OCN1.SGM
12OCN1
Agencies
[Federal Register Volume 81, Number 197 (Wednesday, October 12, 2016)]
[Notices]
[Pages 70423-70425]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-24640]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
Statement of Organization, Functions, and Delegations of
Authority
Part C (Centers for Disease Control and Prevention) of the
Statement of Organization, Functions, and Delegations of Authority of
the Department of Health and Human Services (45 FR 67772-76, dated
October 14, 1980, and corrected at 45 FR 69296, October 20, 1980, as
amended most recently at 81 FR 66284-66285,
[[Page 70424]]
dated September 27, 2016) is amended to reflect the reorganization of
the Division of Scientific Resources, National Center for Emerging and
Zoonotic Infectious Diseases, Office of Infectious Diseases, Centers
for Disease Control and Prevention.
Section C-B, Organization and Functions, is hereby amended as
follows:
Delete and replace the title and the mission and function
statements for the Division of Scientific Resources (CVLH) and insert
the following:
Division of Scientific Resources (CVLH). The Division of Scientific
Resources (DSR) provides products, services, and specialized expertise
to CDC staff and activities in support of research and service
activities: In carrying out its mission, DSR: (1) Provides animals,
laboratory supplies, animal and human blood products, glassware,
mammalian tissue cultures, microbiological media, special reagents, and
other laboratory materials in support of research and service
activities to laboratories and investigators at CDC; (2) develops and
implements applied research programs to expand and enhance the use of
animal models necessary to support research and diagnostic programs and
to improve breeding and husbandry procedures; (3) conducts applied
research in cell biology and in the expansion of tissue culture
technology as a research and diagnostic tool for infectious disease
activities; (4) provides services for laboratory investigators in
protein and DNA synthesis and sequencing, genomic sequencing,
microarrays, proteomics, and molecular modeling; (5) maintains a bank
of serum and other biological specimens of epidemiological and special
significance to CDC's research and diagnostic activities; (6) obtains
and distributes experimental and orphaned vaccines, drugs, antisera,
antitoxins, and immune globulins; (7) manages and distributes the
inventory, maintains the computerized system database, and provides
general technical service support for the dispensing, lyophilizing,
capping, and labeling of CDC reference reagents; (8) receives, triages,
processes, and distributes specimens to CDC laboratories for reference
diagnostic testing, research studies, and epidemics and reports
diagnostic test results to submitting organizations; (9) manages all
CDC exports and ensures compliance with regulations and serves as CDC
liaison with the Department of Commerce for export related issues; (10)
produces and distributes specialized reagents and kits for the
detection of select agents to members of the Laboratory Response
Network; (11) provides services and expertise in development of quality
systems to support compliance with the Food and Drug Administration
regulations on production, distribution, and use of laboratory
diagnostic reagents; (12) provides liaison activities, resources, and
expertise for inquiries related to animals and zoonotic diseases; and
(13) provides a centralized activity for tracking requests for and
distributing select agents to investigators outside of CDC in
compliance with federal regulations.
Office of the Director (CVLH1). (1) Manages, directs, and
coordinates the activities of DSR; (2) provides leadership and guidance
on policy, budget, program planning and development, program
management, and operations; (3) provides DSR-wide administrative and
program services and coordinates or ensures coordination with the
appropriate CIOs, OID, and CDC staff offices on administrative and
program matters; (4) provides liaison with other governmental agencies,
international organizations, and other outside groups; (5) coordinates,
in collaboration with the appropriate CIOs, OID, and CDC components,
laboratory activities relating to support of outbreak investigations or
laboratory-based research including but not limited to specimen
management, biological reagents, and laboratory supplies; (6) maintains
a formulary of investigational and licensed drugs and biologicals that
are distributed to approved physicians for the prevention, control,
and/or treatment of rare, tropical, or exceptional diseases; (7)
advises the Director, NCEZID, on policy matters concerning DSR
activities; and (8) coordinates technical services for laboratory
activities of CDC programs including procurement of glassware and
laboratory supplies.
Comparative Medicine Branch (CVLHB). (1) Acquires and distributes
laboratory animals for research; (2) provides appropriate housing,
husbandry, and psychological enrichment for all research animals; (3)
provides veterinary services, including clinical and surgical support,
for the laboratory animals; (4) develops standard operating procedures
for animal care and use in accordance with the policies established by
the American Association for Accreditation of Laboratory Animal Care,
the Animal Welfare Act, The Guide for the Care & Use of Laboratory
Animals, and the CDC International Animal Care & Use Committee; (5)
conducts applied research to improve the care and use of animals in
research and collaborates on research projects that use laboratory
animals; (6) provides consultation and laboratory animal technology
training to investigators, technical staff and animal care personnel;
(7) provides oversight, support and investigator training for the
graphical animal information technology protocol development and animal
tracking database; (8) coordinates technical services for laboratory
activities of CDC programs including processing and distribution of
glassware and related items, laboratory waste decontamination and
disposal, laundry services, and materiel management; and (9) provides
autoclave label production services.
Biotechnology Core Facility Branch (CVLHD). (1) provides state-of-
the-art next-generation genomic sequencing and metagenomics analysis of
infectious and biothreat agents; (2) provides optical mapping to
produce high resolution whole-genome maps for strain typing, molecular
epidemiology, comparative genomics, and quality control for whole
genome sequence assembly; (3) provides computational analysis of
genomics sequencing data, bioinformatics, and biological computing; (4)
provides qualitative and quantitative proteomic analyses
(identification of expressed proteins by mass spectrometry); analysis
of functionally-relevant post-translational modifications of proteins;
(5) provides mass spectrometry-based positive identification of
bacteria and fungi (BioTyperTM, Bruker Daltonics); (6) provides
synthetic oligonucleotide chemistry in support of development of rapid
diagnostic tests and characterization of pathogens and their hosts; (7)
provides synthetic peptide chemistry in support of studies of immune
response and antigen-antibody interactions; (8) provides biotechnology
seminars and methods evaluation; (9) provides laboratory equipment
design and repair services to all CDC; and (10) collaborates on
research related to STD transmitted infections as chronic infectious
diseases.
Reagent and Diagnostic Services Branch (CVLHG). (1) maintains
laboratory water treatment systems to ensure quality of CDC reagent
grade laboratory water; (2) produces, develops, evaluates and
distributes custom microbiological and cell culture media, buffers and
chemical reagent, mammalian and insect cell cultures, hybridomas,
monoclonal and polycolonal antibodies, and in vitro diagnostic products
for diagnostic research purposes, proficiency testing, pandemic
preparedness, outbreak response and surveillance activities; (3)
collaborates with subject matter experts
[[Page 70425]]
in regulatory compliant development, production, packaging, storing and
distribution of BSL2/BSL3 reagents, select agents, novel immuno-
chemical reagents and reference diagnostic reagents; (4) provides
dispensing, lyophilizing, label production, and device assembly
services; (5) improves the process of bench-top development and in-
house pilot scale production providing immediate availability for
distribution, preventing backorders and streamlining commercialization;
(6) maintains CDC's Biological Reference Reagent Inventory, mammalian
cell line repository and a serviceable inventory at the DSR Continuity
of Operations storage facility; (7) provides centralized specimen
management services for diagnostic, reference, and outbreak
investigations; maintains a bank of biological specimens of
epidemiological significance to CDC's research and diagnostic
activities; manages and tracks systems of specimen collections; (8)
receives, triages, processes, stores and distributes specimens to CDC
laboratories for reference diagnostic testing, research studies, and
reports diagnostic and surveillance test results to submitting
organizations; (9) serves as central facility for acquisition and
distribution of fresh human blood, blood products, and serum in bulk;
(10) packages and ships infectious substances and other materials,
ensuring compliance with regulations for shipping clinical specimens,
infectious substances, and other materials; (11) manages all CDC
exports and ensures compliance with regulations and serves as CDC
liaison with Department of Commerce for export related issues; and (12)
provides consultation in all of the above technical services.
Sherri Berger,
Chief Operating Officer, Centers for Disease Control and Prevention.
[FR Doc. 2016-24640 Filed 10-11-16; 8:45 am]
BILLING CODE 4160-18-P