Charles Jeffrey Edwards: Final Debarment Order, 15481-15482 [2020-05582]
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Federal Register / Vol. 85, No. 53 / Wednesday, March 18, 2020 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2019–N–4046]
Charles Jeffrey Edwards: Final
Debarment Order
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA or Agency) is
issuing an order under the Federal
Food, Drug, and Cosmetic Act (the
FD&C Act) permanently debarring
Charles Jeffrey Edwards from providing
services in any capacity to a person that
has an approved or pending drug
product application. FDA bases this
order on a finding that Mr. Edwards was
convicted, as defined in the FD&C Act,
of two felony counts under federal law
for conduct that relates to the regulation
of a drug product under the FD&C Act.
Mr. Edwards was given notice of the
proposed permanent debarment and
was given an opportunity to request a
hearing within the timeframe prescribed
by regulation to show why he should
not be debarred. As of November 15,
2019 (30 days after receipt of the
notice), Mr. Edwards had not
responded. Mr. Edwards’s failure to
respond and request a hearing
constitutes a waiver of his right to a
hearing concerning this action.
DATES: This order is applicable March
18, 2020.
ADDRESSES: Submit applications for
special termination of debarment to the
Dockets Management Staff (HFA–305),
Food and Drug Administration, 5630
Fishers Lane, Rm. 1061, Rockville, MD
20852.
FOR FURTHER INFORMATION CONTACT:
Jaime Espinosa (ELEM–4029) Division
of Enforcement, Office of Strategic
Planning and Operational Policy, Office
of Regulatory Affairs, Food and Drug
Administration, 12420 Parklawn Dr.,
Rockville, MD 20857, 240–402–8743 or
at debarments@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
SUMMARY:
jbell on DSKJLSW7X2PROD with NOTICES
I. Background
Section 306(a)(2)(B) of the FD&C Act
(21 U.S.C. 335a(a)(2)(B)) requires
debarment of an individual from
providing services in any capacity to a
person that has an approved or pending
drug product application if FDA finds
that the individual has been convicted
of a felony under Federal law for
conduct relating to the regulation of any
drug product under the FD&C Act. On
VerDate Sep<11>2014
18:54 Mar 17, 2020
Jkt 250001
July 20, 2018, Mr. Edwards was
convicted as defined in section
306(l)(1)(A) of the FD&C Act when
judgment was entered against Mr.
Edwards in the U.S. District Court for
the Middle District of Tennessee,
Nashville Division, after his plea of
guilty, to one count of mail fraud in
violation of 18 U.S.C. 1341 and one
count of money laundering in violation
of 18 U.S.C. 1957.
The factual basis for these convictions
is as follows: as contained in Counts 2
and 27 of the Indictment, filed on
January 17, 2013, to which Mr. Edwards
pleaded guilty, from December 2006
through August 2009, Mr. Edwards,
along with others, through Cumberland
Distribution, Inc. (Cumberland), a
company Mr. Edwards co-owned, was
engaged in wholesale distribution of
prescription drugs as defined by section
505(e) of the FD&C Act (21 U.S.C.
355(e)). Cumberland purchased millions
of dollars of prescription drugs from
unlicensed drug suppliers who were not
authorized to distribute drugs under
section 503 of the FD&C Act (21 U.S.C.
353). Mr. Edwards knew that these
unlicensed suppliers often procured
drugs from street level drug diverters
who had obtained the drugs from
persons with legitimate prescriptions.
On many occasions, Mr. Edwards had
drugs shipped to his shell companies,
which Mr. Edwards used as
passthroughs to create the appearance
that his company was purchasing drugs
from licensed suppliers, when in fact
Mr. Edwards was purchasing drugs from
unlicensed suppliers. Afterwards, Mr.
Edwards had these drugs shipped to
Cumberland’s Nashville warehouse
where they were repackaged and
shipped to independent pharmacies
around the country. Mr. Edwards also
directed Cumberland employees to
create false pedigree documents to make
it appear that the diverted drugs were
purchased from authorized sellers. The
diverted drugs included drugs used to
combat human immunodeficiency
virus/acquired immunodeficiency
syndrome; antipsychotic medications;
antidepressants; blood pressure
medications; diabetes medications,
among others. Through the course of
this scheme, Mr. Edwards’ company had
gross proceeds of approximately
$58,984,912. Mr. Edwards and two
others obtained profits of approximately
$14,689,782.
As a result of these convictions, FDA
sent Mr. Edwards by certified mail on
October 9, 2019, a notice proposing to
permanently debar him from providing
services in any capacity to a person that
has an approved or pending drug
product application. The proposal was
PO 00000
Frm 00069
Fmt 4703
Sfmt 4703
15481
based on a finding, under section
306(a)(2)(B) of the FD&C Act, that Mr.
Edwards was convicted of two felonies
under Federal law for conduct relating
to the regulation of a drug product
under the FD&C Act. The proposal also
offered Mr. Edwards an opportunity to
request a hearing, providing him 30
days from the date of receipt of the letter
in which to file the request, and advised
him that failure to request a hearing
constituted an election not to use the
opportunity for a hearing and a waiver
of any contentions concerning this
action. Mr. Edwards received the
proposal on October 16, 2019. Mr.
Edwards did not request a hearing
within the timeframe prescribed by
regulation and has, therefore, waived
his opportunity for a hearing and any
contentions concerning his debarment
(21 CFR part 12).
II. Findings and Order
Therefore, the Assistant
Commissioner, Office of Human and
Animal Food Operations, under section
306(a)(2)(B) of the FD&C Act, under
authority delegated to the Assistant
Commissioner, finds that Mr. Edwards
has been convicted of two felonies
under Federal law for conduct
otherwise relating to the regulation of a
drug product under the FD&C Act.
As a result of the foregoing finding,
Mr. Edwards is permanently debarred
from providing services in any capacity
to a person with an approved or
pending drug product application,
effective (see DATES) (see sections
306(a)(2)(B) and 306(c)(2)(A)(ii) of the
FD&C Act). Any person with an
approved or pending drug product
application who knowingly employs or
retains as a consultant or contractor, or
otherwise uses the services of Mr.
Edwards, in any capacity during his
debarment, will be subject to civil
money penalties (section 307(a)(6) of the
FD&C Act (21 U.S.C. 335b(a)(6))). If Mr.
Edwards provides services in any
capacity to a person with an approved
or pending drug product application
during his period of debarment he will
be subject to civil money penalties
(section 307(a)(7) of the FD&C Act). In
addition, FDA will not accept or review
any abbreviated new drug applications
from Mr. Edwards during his period of
debarment, other than in connection
with an audit under section 306 of the
FD&C Act (section 306(c)(1)(B) of the
FD&C Act). Note that, for purposes of
section 306 of the FD&C Act, a ‘‘drug
product’’ is defined as a ‘‘drug subject
to regulation under section 505, 512, or
802 of this Act [(21 U.S.C. 355, 360b,
382)] or under section 351 of the Public
Health Service Act [(42 U.S.C. 262)]’’
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15482
Federal Register / Vol. 85, No. 53 / Wednesday, March 18, 2020 / Notices
(section 201(dd) of the FD&C Act (21
U.S.C. 321(dd)).
Any application by Mr. Edwards for
special termination of debarment under
section 306(d)(4) of the FD&C Act
should be identified with Docket No.
FDA–2019–N–4046 and sent to the
Dockets Management Staff (see
ADDRESSES). All such submissions are to
be filed in four copies (21 CFR 10.20(a)).
The public availability of information in
these submissions is governed by 21
CFR 10.20.
Publicly available submissions may
be seen in the Dockets Management
Staff between 9 a.m. and 4 p.m.,
Monday through Friday.
Dated: March 12, 2020.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2020–05582 Filed 3–17–20; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
Promoting the Rule of Law Through
Improved Agency Guidance
Documents
Office of the Secretary,
Department of Health and Human
Services.
ACTION: Notice.
AGENCY:
The Department of Health and
Human Services has received an
extension to the deadline to comply
with Executive Order 13891: Promoting
the Rule of Law Through Improved
Agency Guidance Documents. Executive
Order 13891, through Subsections (a)
and (b), requires the establishment of a
new guidance portal and the rescission
of any guidance documents that are not
included in it, respectively. The Office
of Management and Budget (OMB),
through its implementing memorandum
(https://www.whitehouse.gov/wpcontent/uploads/2019/10/M-20-02Guidance-Memo.pdf), has determined
the deadlines for these subsections to be
February 28, 2020. OMB granted the
Department of Health and Human
Services an extension for subsections (a)
and (b) on February 27, 2020. The
Department will establish its guidance
portal by August 31, 2020.
A full copy of the extension letter can
be found on the HHS website at, https://
www.hhs.gov/regulations/.
FOR FURTHER INFORMATION CONTACT:
Samuel Shipley, Office of the Executive
Secretary, at Guidance@hhs.gov or (202)
690–5627.
jbell on DSKJLSW7X2PROD with NOTICES
SUMMARY:
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18:54 Mar 17, 2020
Jkt 250001
Dated: March 12, 2020.
Ann C. Agnew,
Executive Secretary, Department of Health
and Human Services.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[FR Doc. 2020–05647 Filed 3–17–20; 8:45 am]
Center for Scientific Review; Amended
Notice of Meeting
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Heart, Lung, and Blood
Institute; Notice of Closed Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
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: National Heart, Lung,
and Blood Institute Special Emphasis Panel;
R13 Conference Grants.
Date: April 14, 2020.
Time: 8:30 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: NIH/NHLBI, Rockledge I, 6705
Rockledge Drive, Bethesda, MD 20814
(Virtual Meeting).
Contact Person: Michael P. Reilly, Ph.D.,
Scientific Review Officer, Office of Scientific
Review, National Heart, Lung, and Blood
Institute, National Institutes of Health, 6705
Rockledge Drive, Bethesda, MD 20892, 301–
827–7975, reillymp@nhlbi.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.233, National Center for
Sleep Disorders Research; 93.837, Heart and
Vascular Diseases Research; 93.838, Lung
Diseases Research; 93.839, Blood Diseases
and Resources Research, National Institutes
of Health, HHS)
Dated: March 13, 2020.
Ronald J. Livingston, Jr.,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2020–05626 Filed 3–17–20; 8:45 am]
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National Institutes of Health
Notice is hereby given of a change in
the meeting of the Center for Scientific
Review Special Emphasis Panel,
Fellowships: Physiology and
Pathobiology of the Vascular and
Hematological Systems, March 27, 2020
8:00 a.m. to March 27, 2020, 8:00 p.m.,
The William F. Bolger Center, 9600
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which was published in the Federal
Register on March 4, 2020, 85 FR 12799.
The meeting location is being held at
the National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892.
The meeting date and time remains the
same. The meeting is closed to the
public.
Dated: March 13, 2020.
Melanie J. Pantoja,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2020–05637 Filed 3–17–20; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Allergy and
Infectious Diseases; Notice of Closed
Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, 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
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The contract proposals and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the contract
proposals, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Institute of
Allergy and Infectious Diseases Special
Emphasis Panel HHS–NIH–CDC–SBIR 2018–
1 Phase II Topic 053: Effective Targeted
Delivery of RNA-based Vaccines and
Therapeutics.
Date: April 15, 2020.
Time: 2:00 p.m. to 5:00 p.m.
Agenda: To review and evaluate contract
proposals.
Place: National Institute of Allergy and
Infectious Diseases, National Institutes of
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Agencies
[Federal Register Volume 85, Number 53 (Wednesday, March 18, 2020)]
[Notices]
[Pages 15481-15482]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-05582]
[[Page 15481]]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2019-N-4046]
Charles Jeffrey Edwards: Final Debarment Order
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA or Agency) is issuing an
order under the Federal Food, Drug, and Cosmetic Act (the FD&C Act)
permanently debarring Charles Jeffrey Edwards from providing services
in any capacity to a person that has an approved or pending drug
product application. FDA bases this order on a finding that Mr. Edwards
was convicted, as defined in the FD&C Act, of two felony counts under
federal law for conduct that relates to the regulation of a drug
product under the FD&C Act. Mr. Edwards was given notice of the
proposed permanent debarment and was given an opportunity to request a
hearing within the timeframe prescribed by regulation to show why he
should not be debarred. As of November 15, 2019 (30 days after receipt
of the notice), Mr. Edwards had not responded. Mr. Edwards's failure to
respond and request a hearing constitutes a waiver of his right to a
hearing concerning this action.
DATES: This order is applicable March 18, 2020.
ADDRESSES: Submit applications for special termination of debarment to
the Dockets Management Staff (HFA-305), Food and Drug Administration,
5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT: Jaime Espinosa (ELEM-4029) Division of
Enforcement, Office of Strategic Planning and Operational Policy,
Office of Regulatory Affairs, Food and Drug Administration, 12420
Parklawn Dr., Rockville, MD 20857, 240-402-8743 or at
[email protected].
SUPPLEMENTARY INFORMATION:
I. Background
Section 306(a)(2)(B) of the FD&C Act (21 U.S.C. 335a(a)(2)(B))
requires debarment of an individual from providing services in any
capacity to a person that has an approved or pending drug product
application if FDA finds that the individual has been convicted of a
felony under Federal law for conduct relating to the regulation of any
drug product under the FD&C Act. On July 20, 2018, Mr. Edwards was
convicted as defined in section 306(l)(1)(A) of the FD&C Act when
judgment was entered against Mr. Edwards in the U.S. District Court for
the Middle District of Tennessee, Nashville Division, after his plea of
guilty, to one count of mail fraud in violation of 18 U.S.C. 1341 and
one count of money laundering in violation of 18 U.S.C. 1957.
The factual basis for these convictions is as follows: as contained
in Counts 2 and 27 of the Indictment, filed on January 17, 2013, to
which Mr. Edwards pleaded guilty, from December 2006 through August
2009, Mr. Edwards, along with others, through Cumberland Distribution,
Inc. (Cumberland), a company Mr. Edwards co-owned, was engaged in
wholesale distribution of prescription drugs as defined by section
505(e) of the FD&C Act (21 U.S.C. 355(e)). Cumberland purchased
millions of dollars of prescription drugs from unlicensed drug
suppliers who were not authorized to distribute drugs under section 503
of the FD&C Act (21 U.S.C. 353). Mr. Edwards knew that these unlicensed
suppliers often procured drugs from street level drug diverters who had
obtained the drugs from persons with legitimate prescriptions. On many
occasions, Mr. Edwards had drugs shipped to his shell companies, which
Mr. Edwards used as passthroughs to create the appearance that his
company was purchasing drugs from licensed suppliers, when in fact Mr.
Edwards was purchasing drugs from unlicensed suppliers. Afterwards, Mr.
Edwards had these drugs shipped to Cumberland's Nashville warehouse
where they were repackaged and shipped to independent pharmacies around
the country. Mr. Edwards also directed Cumberland employees to create
false pedigree documents to make it appear that the diverted drugs were
purchased from authorized sellers. The diverted drugs included drugs
used to combat human immunodeficiency virus/acquired immunodeficiency
syndrome; antipsychotic medications; antidepressants; blood pressure
medications; diabetes medications, among others. Through the course of
this scheme, Mr. Edwards' company had gross proceeds of approximately
$58,984,912. Mr. Edwards and two others obtained profits of
approximately $14,689,782.
As a result of these convictions, FDA sent Mr. Edwards by certified
mail on October 9, 2019, a notice proposing to permanently debar him
from providing services in any capacity to a person that has an
approved or pending drug product application. The proposal was based on
a finding, under section 306(a)(2)(B) of the FD&C Act, that Mr. Edwards
was convicted of two felonies under Federal law for conduct relating to
the regulation of a drug product under the FD&C Act. The proposal also
offered Mr. Edwards an opportunity to request a hearing, providing him
30 days from the date of receipt of the letter in which to file the
request, and advised him that failure to request a hearing constituted
an election not to use the opportunity for a hearing and a waiver of
any contentions concerning this action. Mr. Edwards received the
proposal on October 16, 2019. Mr. Edwards did not request a hearing
within the timeframe prescribed by regulation and has, therefore,
waived his opportunity for a hearing and any contentions concerning his
debarment (21 CFR part 12).
II. Findings and Order
Therefore, the Assistant Commissioner, Office of Human and Animal
Food Operations, under section 306(a)(2)(B) of the FD&C Act, under
authority delegated to the Assistant Commissioner, finds that Mr.
Edwards has been convicted of two felonies under Federal law for
conduct otherwise relating to the regulation of a drug product under
the FD&C Act.
As a result of the foregoing finding, Mr. Edwards is permanently
debarred from providing services in any capacity to a person with an
approved or pending drug product application, effective (see DATES)
(see sections 306(a)(2)(B) and 306(c)(2)(A)(ii) of the FD&C Act). Any
person with an approved or pending drug product application who
knowingly employs or retains as a consultant or contractor, or
otherwise uses the services of Mr. Edwards, in any capacity during his
debarment, will be subject to civil money penalties (section 307(a)(6)
of the FD&C Act (21 U.S.C. 335b(a)(6))). If Mr. Edwards provides
services in any capacity to a person with an approved or pending drug
product application during his period of debarment he will be subject
to civil money penalties (section 307(a)(7) of the FD&C Act). In
addition, FDA will not accept or review any abbreviated new drug
applications from Mr. Edwards during his period of debarment, other
than in connection with an audit under section 306 of the FD&C Act
(section 306(c)(1)(B) of the FD&C Act). Note that, for purposes of
section 306 of the FD&C Act, a ``drug product'' is defined as a ``drug
subject to regulation under section 505, 512, or 802 of this Act [(21
U.S.C. 355, 360b, 382)] or under section 351 of the Public Health
Service Act [(42 U.S.C. 262)]''
[[Page 15482]]
(section 201(dd) of the FD&C Act (21 U.S.C. 321(dd)).
Any application by Mr. Edwards for special termination of debarment
under section 306(d)(4) of the FD&C Act should be identified with
Docket No. FDA-2019-N-4046 and sent to the Dockets Management Staff
(see ADDRESSES). All such submissions are to be filed in four copies
(21 CFR 10.20(a)). The public availability of information in these
submissions is governed by 21 CFR 10.20.
Publicly available submissions may be seen in the Dockets
Management Staff between 9 a.m. and 4 p.m., Monday through Friday.
Dated: March 12, 2020.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2020-05582 Filed 3-17-20; 8:45 am]
BILLING CODE 4164-01-P