Glenn R. Unger, D.D.S.; Declaratory Order, 49339-49340 [2014-19785]
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Federal Register / Vol. 79, No. 161 / Wednesday, August 20, 2014 / Notices
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38. Accordingly, the Commission finds
no violation of section 337 as to the
asserted claims of the ’151 patent,
namely independent claims 1 and 16,
and asserted claims dependent upon
them.
The Commission has determined not
to review the final ID’s determination
that claim 16 of the ’151 patent is
invalid for indefiniteness. Final ID at
29–31; see IA Pet. 6–12; InterDigital Pet.
24–29; see also Rembrandt Data Techs.,
LP v. AOL, LLC, 641 F.3d 1331, 1339–
40 (Fed. Cir. 2011). Accordingly, there
can be no violation of section 337 as to
claim 16 and its asserted dependent
claims.
The Commission has determined to
review the final ID’s construction of
‘‘and to’’ in claim 16 of the ’151 patent,
Final ID at 31–34; see InterDigital Pet.
at 29–33, and on review finds that the
term is to be afforded its plain and
ordinary meaning. In view of the
Commission’s claim construction, the
final ID’s finding of noninfringement of
asserted claims 16–21 and 23–24 based
upon the final ID’s construction, Final
ID at 58–60, is reversed. The
Commission has also determined to
review the final ID’s infringement
analysis of ‘‘and if so’’ for claim 1, Final
ID at 58–60; see InterDigital Pet. at 38–
43, and on review takes no position
whether the accused products practice
the determining steps in sequence as
required for asserted claims 1–6 and 8–
9.
3. Domestic Industry, FRAND, and
Other Issues
Except as recited above concerning
the Commission’s finding that the
domestic industry products do not
practice the asserted patent claims, the
Commission reviews and takes no
position on the remaining domestic
industry issues raised in the parties’
petitions. Similarly, the Commission
reviews and takes no position on the
FRAND issues raised by the respondents
concerning their affirmative defenses.
The Commission finds that it is in the
interest of the efficient use of
administrative, judicial, and private
resources for the domestic industry and
FRAND issues to be decided, if at all,
subsequent to final disposition of the
pending appeal in InterDigital
Communications LLC v. ITC, No. 2014–
1176 (Fed. Cir.), which involves many
of the same parties and issues with
regard to related patents.
The Commission does not review any
other issues raised in the parties’
petitions except as otherwise recited
above. The reasoning in support of the
Commission’s decision will be set forth
in fuller detail in a forthcoming opinion.
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16:44 Aug 19, 2014
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The authority for the Commission’s
determination is contained in section
337 of the Tariff Act of 1930, as
amended (19 U.S.C. 1337), and in Part
210 of the Commission’s Rules of
Practice and Procedure (19 CFR part
210).
By order of the Commission.
Issued: August 14, 2014.
Lisa R. Barton,
Secretary to the Commission.
[FR Doc. 2014–19715 Filed 8–19–14; 8:45 am]
BILLING CODE 7020–02–P
INTERNATIONAL TRADE
COMMISSION
[Investigation Nos. 701–TA–505 and 731–
TA–1231, 1232, 1235, and 1237 (Final)]
Grain-Oriented Electrical Steel
(‘‘GOES’’) From China, Czech
Republic, Korea, and Russia
Supplemental schedule for the subject
investigations.
AGENCY: United States International
Trade Commission.
ACTION: Notice.
DATES:
Effective Date: August 13, 2014.
FOR FURTHER INFORMATION CONTACT:
Mary Messer (202–205–3193), Office of
Investigations, U.S. International Trade
Commission, 500 E Street SW.,
Washington, DC 20436. Hearingimpaired persons can obtain
information on this matter by contacting
the Commission’s TDD terminal on 202–
205–1810. Persons with mobility
impairments who will need special
assistance in gaining access to the
Commission should contact the Office
of the Secretary at 202–205–2000.
General information concerning the
Commission may also be obtained by
accessing its internet server (https://
www.usitc.gov). The public record for
these investigations may be viewed on
the Commission’s electronic docket
(EDIS) at https://edis.usitc.gov.
SUPPLEMENTARY INFORMATION: Effective
May 9, 2013, the Commission
established a schedule for the conduct
of the final phase of the subject
investigations (79 FR 32310, June 4,
2014). The Department of Commerce
extended the date for its final
determinations in the investigations
concerning China, Czech Republic,
Korea, and Russia to no later than 135
days after the publication of the
preliminary determinations (79 FR
26936, May 12, 2014 (China); 79 FR
26717, May 9, 2014 (Czech Republic);
79 FR 26939, May 12, 2014 (Korea); and
79 FR 26941, May 12, 2014 (Russia)).
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49339
The Commission, therefore, is
supplementing its schedule to conform
with Commerce’s postponed schedule.
The Commission’s supplemental
schedule for the investigations is as
follows: the deadline for filing party
comments on Commerce’s final
determinations is October 2, 2014; the
staff report in the final phase of these
investigations will be placed in the
nonpublic record on October 14, 2014,
and a public version will be issued
thereafter.
Supplemental party comments may
address only Commerce’s final
determinations regarding imports from
China, Czech Republic, Korea, and
Russia. These supplemental final
comments may not contain new factual
information and may not exceed five (5)
pages in length.
For further information concerning
these investigations see the
Commission’s notice cited above and
the Commission’s Rules of Practice and
Procedure, part 201, subparts A through
E (19 CFR part 201), and part 207,
subparts A and C (19 CFR part 207).
Authority: These investigations are being
conducted under authority of title VII of the
Tariff Act of 1930; this notice is published
pursuant to section 207.21 of the
Commission’s rules.
By order of the Commission.
Issued: August 14, 2014.
Lisa R. Barton,
Secretary to the Commission.
[FR Doc. 2014–19716 Filed 8–19–14; 8:45 am]
BILLING CODE 7020–02–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Glenn R. Unger, D.D.S.; Declaratory
Order
On March 7, 2014, the Deputy
Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration, issued an Order to
Show Cause to Glenn R. Unger, D.D.S.,
of Clifton Park, New York. The Show
Cause Order proposed the revocation of
the Certificate of Registration issued to
Dr. Unger on three separate grounds.
First, the Show Cause Order alleged
that Dr. Unger’s New York State dental
license expired on June 30, 2010, and
that he is ‘‘currently without authority
to practice dentistry or handle
controlled substances in the State of
New York, the State in which [he is]
registered with the DEA.’’ GX 1, at 1–2.
The Order thus alleged that Dr. Unger’s
registration is subject to revocation
under 21 U.S.C. 824(a)(3). Id. at 2.
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49340
Federal Register / Vol. 79, No. 161 / Wednesday, August 20, 2014 / Notices
Second, the Show Cause Order
alleged that on June 25, 2012, Dr. Unger
submitted an application to renew his
DEA registration. Id. The Order alleged
that notwithstanding that his New York
State dental license had expired on June
30, 2010, Dr. Unger falsely stated that
his license did not expire until June 30,
2013. Id. The Order thus alleged that
this constituted a material falsification
of the application and was ground to
revoke the registration under 21 U.S.C.
824(a)(1).
Third, the Show Cause Order alleged
that notwithstanding his lack of state
authority to dispense controlled
substances, ‘‘between December 2010
and November 2012,’’ Dr. Unger ‘‘issued
at least seven controlled substance
prescriptions’’ to L.B. and M.N., for
drugs which included hydrocodone 10/
325mg, Ambien 10mg, and Percocet 5/
325mg. Id. The Order further alleged
that Dr. Unger violated federal law by
authorizing six refills for two of the
hydrocodone prescriptions and twelve
refills for an Ambien prescription. Id.
(citing 21 U.S.C. 829(b) and 21 CFR
1306.22(a)). Finally, the Order alleged
that Dr. Unger violated federal law
which prohibits the refilling of a
schedule II prescription when he
authorized two refills of a Percocet
prescription. Id. at 3 (citing 21 U.S.C.
829(a) and 21 CFR 1306.12(a)). The
Order thus alleged that Dr. Unger had
committed acts rendering his
registration ‘‘inconsistent with the
public interest.’’ 21 U.S.C. 824(a)(4).
The Show Cause Order also notified
Dr. Unger of his right to request a
hearing on the allegations or to submit
a written statement in lieu of a hearing,
the procedure for electing either option,
and the consequence of failing to elect
either option. GX 1, at 3 (citing 21 CFR
1301.43). On March 11, 2014, a DEA
Diversion Investigator (DI) personally
served the Show Cause Order on Dr.
Unger who was then incarcerated at the
Rennselaer County Jail. GX 3.
Since the date of service, thirty (30)
days have now passed and neither Dr.
Unger, nor anyone purporting to
represent him, has requested a hearing
on the allegations or submitted a written
statement in lieu of a hearing. I therefore
find that Dr. Unger has waived his right
to a hearing or to submit a written
statement and issue this Decision and
Order based on evidence contained in
the Investigative Record submitted by
the Government. 21 CFR 1301.43(d) &
(e). I make the following findings of fact.
Findings
Dr. Unger was licensed as a dentist by
the State of New York between July 16,
1976 and June 30, 2010, at which point
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16:44 Aug 19, 2014
Jkt 232001
he became unregistered to practice
dentistry. GX 4. Dr. Unger remains
unregistered by the State as of the date
of this order.
Dr. Unger also previously held DEA
Certificate of Registration FU1504477,
pursuant to which he was authorized to
dispense controlled substances as a
practitioner in schedules II through V.
GX 6. While this registration apparently
expired in May 2012, on June 22, 2012,
a renewal application was submitted for
this registration. Id. The application
listed Dr. Unger’s former New York
State license number and provided an
expiration date of June 30, 2013. Id. at
2; GX 5, at 1. The application was not,
however, signed by Dr. Unger but by a
person named ‘‘Nathan Green.’’ GX 5,
at 2.
Notably, the Application contains the
following statement immediately above
the signature line: ‘‘Name of Applicant
(For Individual registrants, the registrant
themselves MUST complete this ESignature).’’ Id. Moreover, immediately
below the E-Signature line, the
Application contains the following
statement: ‘‘This electronic application/
DEA form must be certified by the
applicant/registrant, if an
individual . . . .’’ Id.
Discussion
Under DEA regulations:
[e]ach application, attachment, or other
document filed as part of an application,
shall be signed by the applicant, if an
individual. . . . An applicant may authorize
one or more individuals, who would not
otherwise be authorized to do so, to sign
applications for the applicant by filing with
the Registration Unit of the Administration a
power of attorney for each such individual.
The power of attorney shall be signed by a
person who is authorized to sign applications
under this paragraph and shall contain the
signature of the individual being authorized
to sign applications.
21 CFR 1301.13(j).
As found above, Dr. Unger did not
sign the application. Moreover,
according to the registration records of
the Agency (of which I take official
notice, see 5 U.S.C. 556(e)), Dr. Unger
has not submitted a power of attorney
designating any person as authorized to
sign his application. Accordingly, I find
that the June 22, 2012 application was
defective and should not have been
accepted for filing. I further declare that
DEA Certificate of Registration
FU1504477 issued to Dr. Glenn R. Unger
on June 25, 2012, was void ab initio and
order that the registration be terminated.
See id. § 554(e). There being no
application to act upon or registration to
revoke, I further order that the Order to
Show Cause be dismissed.
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It is so ordered.
Dated: August 7, 2014.
Thomas M. Harrigan,
Deputy Administrator.
[FR Doc. 2014–19785 Filed 8–19–14; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–396]
Electronic Prescriptions for Controlled
Substances Notice of Approved
Certification Process
Drug Enforcement
Administration, Department of Justice.
ACTION: Notice.
AGENCY:
The Drug Enforcement
Administration (DEA) is announcing
one new DEA-approved certification
process for providers of Electronic
Prescriptions for Controlled Substances
(EPCS) applications. Certifying
organizations with a certification
process approved pursuant to 21 CFR
1311.300(e) are posted on DEA’s Web
site upon approval.
FOR FURTHER INFORMATION CONTACT:
Imelda L. Paredes, Office of Diversion
Control, Drug Enforcement
Administration; Mailing Address: 8701
Morrissette Drive, Springfield, Virginia
22152, Telephone: (202) 598–6812.
SUPPLEMENTARY INFORMATION:
SUMMARY:
Legal Authority
The DEA implements and enforces
titles II and III of the Comprehensive
Drug Abuse Prevention and Control Act
of 1970, as amended. Titles II and III are
referred to as the ‘‘Controlled
Substances Act’’ and the ‘‘Controlled
Substances Import and Export Act,’’
respectively, and are collectively
referred to as the ‘‘Controlled
Substances Act’’ or the ‘‘CSA’’ for the
purpose of this notice. 21 U.S.C. 801–
971. The DEA publishes the
implementing regulations for these
statutes in title 21 of the Code of Federal
Regulations (CFR), parts 1300 to 1321.
The CSA and its implementing
regulations are designed to prevent,
detect, and eliminate the diversion of
controlled substances and listed
chemicals into the illicit market while
providing for the legitimate medical,
scientific, research, and industrial needs
of the United States. Controlled
substances have the potential for abuse
and dependence and are controlled to
protect the public health and safety.
The CSA and DEA’s implementing
regulations establish the legal
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Agencies
[Federal Register Volume 79, Number 161 (Wednesday, August 20, 2014)]
[Notices]
[Pages 49339-49340]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-19785]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Glenn R. Unger, D.D.S.; Declaratory Order
On March 7, 2014, the Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement Administration, issued an Order to
Show Cause to Glenn R. Unger, D.D.S., of Clifton Park, New York. The
Show Cause Order proposed the revocation of the Certificate of
Registration issued to Dr. Unger on three separate grounds.
First, the Show Cause Order alleged that Dr. Unger's New York State
dental license expired on June 30, 2010, and that he is ``currently
without authority to practice dentistry or handle controlled substances
in the State of New York, the State in which [he is] registered with
the DEA.'' GX 1, at 1-2. The Order thus alleged that Dr. Unger's
registration is subject to revocation under 21 U.S.C. 824(a)(3). Id. at
2.
[[Page 49340]]
Second, the Show Cause Order alleged that on June 25, 2012, Dr.
Unger submitted an application to renew his DEA registration. Id. The
Order alleged that notwithstanding that his New York State dental
license had expired on June 30, 2010, Dr. Unger falsely stated that his
license did not expire until June 30, 2013. Id. The Order thus alleged
that this constituted a material falsification of the application and
was ground to revoke the registration under 21 U.S.C. 824(a)(1).
Third, the Show Cause Order alleged that notwithstanding his lack
of state authority to dispense controlled substances, ``between
December 2010 and November 2012,'' Dr. Unger ``issued at least seven
controlled substance prescriptions'' to L.B. and M.N., for drugs which
included hydrocodone 10/325mg, Ambien 10mg, and Percocet 5/325mg. Id.
The Order further alleged that Dr. Unger violated federal law by
authorizing six refills for two of the hydrocodone prescriptions and
twelve refills for an Ambien prescription. Id. (citing 21 U.S.C. 829(b)
and 21 CFR 1306.22(a)). Finally, the Order alleged that Dr. Unger
violated federal law which prohibits the refilling of a schedule II
prescription when he authorized two refills of a Percocet prescription.
Id. at 3 (citing 21 U.S.C. 829(a) and 21 CFR 1306.12(a)). The Order
thus alleged that Dr. Unger had committed acts rendering his
registration ``inconsistent with the public interest.'' 21 U.S.C.
824(a)(4).
The Show Cause Order also notified Dr. Unger of his right to
request a hearing on the allegations or to submit a written statement
in lieu of a hearing, the procedure for electing either option, and the
consequence of failing to elect either option. GX 1, at 3 (citing 21
CFR 1301.43). On March 11, 2014, a DEA Diversion Investigator (DI)
personally served the Show Cause Order on Dr. Unger who was then
incarcerated at the Rennselaer County Jail. GX 3.
Since the date of service, thirty (30) days have now passed and
neither Dr. Unger, nor anyone purporting to represent him, has
requested a hearing on the allegations or submitted a written statement
in lieu of a hearing. I therefore find that Dr. Unger has waived his
right to a hearing or to submit a written statement and issue this
Decision and Order based on evidence contained in the Investigative
Record submitted by the Government. 21 CFR 1301.43(d) & (e). I make the
following findings of fact.
Findings
Dr. Unger was licensed as a dentist by the State of New York
between July 16, 1976 and June 30, 2010, at which point he became
unregistered to practice dentistry. GX 4. Dr. Unger remains
unregistered by the State as of the date of this order.
Dr. Unger also previously held DEA Certificate of Registration
FU1504477, pursuant to which he was authorized to dispense controlled
substances as a practitioner in schedules II through V. GX 6. While
this registration apparently expired in May 2012, on June 22, 2012, a
renewal application was submitted for this registration. Id. The
application listed Dr. Unger's former New York State license number and
provided an expiration date of June 30, 2013. Id. at 2; GX 5, at 1. The
application was not, however, signed by Dr. Unger but by a person named
``Nathan Green.'' GX 5, at 2.
Notably, the Application contains the following statement
immediately above the signature line: ``Name of Applicant (For
Individual registrants, the registrant themselves MUST complete this E-
Signature).'' Id. Moreover, immediately below the E-Signature line, the
Application contains the following statement: ``This electronic
application/DEA form must be certified by the applicant/registrant, if
an individual . . . .'' Id.
Discussion
Under DEA regulations:
[e]ach application, attachment, or other document filed as part
of an application, shall be signed by the applicant, if an
individual. . . . An applicant may authorize one or more
individuals, who would not otherwise be authorized to do so, to sign
applications for the applicant by filing with the Registration Unit
of the Administration a power of attorney for each such individual.
The power of attorney shall be signed by a person who is authorized
to sign applications under this paragraph and shall contain the
signature of the individual being authorized to sign applications.
21 CFR 1301.13(j).
As found above, Dr. Unger did not sign the application. Moreover,
according to the registration records of the Agency (of which I take
official notice, see 5 U.S.C. 556(e)), Dr. Unger has not submitted a
power of attorney designating any person as authorized to sign his
application. Accordingly, I find that the June 22, 2012 application was
defective and should not have been accepted for filing. I further
declare that DEA Certificate of Registration FU1504477 issued to Dr.
Glenn R. Unger on June 25, 2012, was void ab initio and order that the
registration be terminated. See id. Sec. 554(e). There being no
application to act upon or registration to revoke, I further order that
the Order to Show Cause be dismissed.
It is so ordered.
Dated: August 7, 2014.
Thomas M. Harrigan,
Deputy Administrator.
[FR Doc. 2014-19785 Filed 8-19-14; 8:45 am]
BILLING CODE 4410-09-P