Office of the Secretary, Health Care Fraud and Abuse Data Collection Program: Reporting of Final Adverse Actions; Correction, 36554-36555 [05-12481]
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36554
Federal Register / Vol. 70, No. 121 / Friday, June 24, 2005 / Proposed Rules
TABLE 1.—WASTES EXCLUDED FROM NON-SPECIFIC SOURCES—Continued
Facility
Address
Waste description
(6) Reopener Language: (A) If, at any time after disposal of the delisted waste, Nissan possesses or is otherwise made aware of any environmental data (including
but not limited to leachate data or groundwater monitoring data) or any other data
relevant to the delisted waste indicating that any constituent identified in the
delisting verification testing is at a level higher than the delisting level allowed by
EPA in granting the petition, Nissan must report the data, in writing, to EPA within
10 days of first possessing or being made aware of that data. (B) If the testing of
the waste, as required by Condition (2)(B), does not meet the delisting requirements of Condition (1), Nissan must report the data, in writing, to EPA within 10
days of first possessing or being made aware of that data. (C) Based on the information described in paragraphs (6)(A) or (6)(B) and any other information received from any source, EPA will make a preliminary determination as to whether
the reported information requires that EPA take action to protect human health or
the environment. Further action may include suspending or revoking the exclusion, or other appropriate response necessary to protect human health and the
environment. (D) If EPA determines that the reported information does require
Agency action, EPA will notify the facility in writing of the action believed necessary to protect human health and the environment. The notice shall include a
statement of the proposed action and a statement providing Nissan with an opportunity to present information as to why the proposed action is not necessary. Nissan shall have 10 days from the date of EPA’s notice to present such information.
(E) Following the receipt of information from Nissan, as described in paragraph
(6)(D), or if no such information is received within 10 days, EPA will issue a final
written determination describing the Agency actions that are necessary to protect
human health or the environment, given the information received in accordance
with paragraphs (6)(A) or (6)(B). Any required action described in EPA’s determination shall become effective immediately, unless EPA provides otherwise.
(7) Notification Requirements: Nissan must provide a one-time written notification to
any State Regulatory Agency in a State to which or through which the delisted
waste described above will be transported, at least 60 days prior to the commencement of such activities. Failure to provide such a notification will result in a
violation of the delisting conditions and a possible revocation of the decision to
delist.
*
*
*
[FR Doc. 05–12579 Filed 6–23–05; 8:45 am]
BILLING CODE 6560–50–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of Inspector General
45 CFR Part 61
RIN 0906–AA46
Office of the Secretary, Health Care
Fraud and Abuse Data Collection
Program: Reporting of Final Adverse
Actions; Correction
Office of Inspector General
(OIG), HHS.
ACTION: Proposed correction
amendment.
AGENCY:
SUMMARY: This document proposes a
correction to the final regulations,
which were published in the Federal
Register on October 26, 1999 (64 FR
57740). These regulations established a
national health care fraud and abuse
data collection program for the reporting
and disclosing of certain adverse actions
taken against health care providers,
VerDate jul<14>2003
16:57 Jun 23, 2005
Jkt 205001
*
*
suppliers and practitioners, and for
maintaining a data base of final adverse
actions taken against health care
providers, suppliers and practitioners.
An inadvertent error appeared in the
text of the regulations concerning the
definition of the term ‘‘any other
negative action or finding.’’ As a result,
we are proposing to correct 45 CFR 61.3,
Definitions, to assure the technical
correctness of these regulations.
DATES: To assure consideration, public
comments must be mailed and delivered
to the address provided below by no
later than 5 p.m., July 25, 2005.
ADDRESSES: Please mail or deliver your
written comments to the following
address: Department of Health and
Human Services, Office of Inspector
General, Attention: OIG–46–CA2, 330
Independence Avenue, SW., Room
5246, Washington, DC 20201.
FOR FURTHER INFORMATION CONTACT: Joel
Schaer, OIG Regulations Officer Office
of External Affairs, (202) 619–0089.
SUPPLEMENTARY INFORMATION: The HHS
Office of Inspector General (OIG) issued
final regulations on October 26, 1999
(64 FR 57740) that established a
national health care fraud and abuse
PO 00000
Frm 00019
Fmt 4702
Sfmt 4702
*
*
data collection program—the Healthcare
Integrity and Protection Data Bank
(HIPDB)—for the reporting and
disclosing of certain final adverse
actions taken against health care
providers, suppliers and practitioners,
and for maintaining a data base of final
adverse actions taken against health care
providers, suppliers and practitioners.
The final rule established a new 45 CFR
part 61 to implement the requirements
for reporting of specific data elements
to, and procedures for obtaining
information from, the HIPDB. In that
final rule, an inadvertent error appeared
in § 61.3—the definitions section of the
regulations—and is now being proposed
for correction.
Section 61.3 expanded on previous
regulatory definitions and provided
additional examples of the scope of
various terms set fort in the statute. On
page 57755 of the preamble,
summarizing the various revisions being
made to the final rule, we indicated that
with respect to the definition for the
term ‘‘any other negative action or
finding’’ there are certain kinds of
actions or findings that would not meet
the intent of the statute and not be
E:\FR\FM\24JNP1.SGM
24JNP1
Federal Register / Vol. 70, No. 121 / Friday, June 24, 2005 / Proposed Rules
reportable. We cited, as an example,
administrative actions, such as limited
training permits, limited licenses for
telemedicine, fines or citations that do
not restrict a practitioner’s practice, or
personnel actions for tardiness, that
were not within the range of actions
intended by the statute. As a result, we
agreed to add a clarifying phrase to this
term. The revised definition would
exclude administrative fines or
citations, corrective action plans and
other personnel actions, unless they are
(1) connected to the billing, provision or
delivery of health care services, and (2)
taken in conjunction with other
licensure or certification actions such as
revocation, suspension, censure,
reprimand, probation, or surrender.
However, we inadvertently omitted this
clarifying language to the regulations
text of the rule itself. Therefore, to be
consistent with the intended
clarification and the overall intent of the
final rulemaking, we are correcting this
inadvertent error in the definition of the
term ‘‘any other negative action or
finding’’ that appeared on page 57759 in
the October 26, 1999 final regulations to
include this additional clarifying
language.
Comments should be addressed
specifically to the issue of clarifying the
existing definition of the term in
question in accordance with the earlier
final rulemaking.
Response to Public Comments
Comments will be available for public
inspection beginning on July 8, 2005 in
Room 5518 of the Office of Inspector
General at 330 Independence Avenue,
SW., Washington DC, on Monday
through Friday of each week from 8 a.m.
to 4 p.m., (202) 619–0089. Because of
the number of comments we normally
receive on regulations, we will not
acknowledge or respond to them
individually. However, we will consider
all timely and appropriate comments
when developing the final corrections
amendment.
Billing and transportation services,
Durable medical equipment suppliers
and manufacturers, Health care insurers,
Health maintenance organizations,
Health professions, Home health care
agencies, Hospitals, Penalties,
Pharmaceutical suppliers and
manufacturers, Privacy, Reporting and
recordkeeping requirements, Skilled
nursing facilities.
Therefore, 45 CFR part 61 is proposed
to be amended by making the following
correcting amendment:
16:57 Jun 23, 2005
Jkt 205001
1. The authority citation for part 61
would continue to read as follows:
Authority: 42 U.S.C. 1320a-7e.
2. Section 61.3 would be amended by
republishing the introductory text, and
by revising the definition for the term
‘‘Any other negative action or finding’’
to read as follows:
§ 61.3
Definitions.
The following definitions apply to
this part:
*
*
*
*
*
Any other negative action or finding
by a Federal or State licensing agency
means any action or finding that under
the State’s law is publicly available
information, and rendered by a
licensing authority, including but not
limited to, limitations on the scope of
practice, liquidations, injunctions and
forfeitures. This definition also includes
final adverse actions rendered by a
Federal or State licensing or
certification authority, such as
exclusions, revocations or suspension of
license or certification that occur in
conjunction with settlements in which
no finding of liability has been made
(although such a settlement itself is not
reportable under the statute). This
definition excludes administrative fines
or citations and corrective action plans
and other personnel actions, unless they
are:
(1) Connected to the delivery of health
care services; and
(2) taken in conjunction with other
licensure or certification actions such as
revocation, suspension, censure,
reprimand, probation or surrender.
*
*
*
*
*
Dated: June 20, 2005.
Ann Agnew,
Executive Secretary to the Department.
[FR Doc. 05–12481 Filed 6–23–05; 8:45 am]
BILLING CODE 4152–01–P
List of Subjects in 45 CFR Part 61
VerDate jul<14>2003
PART 61—HEALTHCARE INTEGRITY
AND PROTECTION DATA BANK FOR
FINAL ADVERSE INFORMATION ON
HEALTH CARE PROVIDERS,
SUPPLIERS AND PRACTITIONERS
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
50 CFR Part 679
[I.D. 062005A]
Fisheries of the Exclusive Economic
Zone Off Alaska; Public Workshop
National Marine Fisheries
Service (NMFS), National Oceanic and
AGENCY:
PO 00000
Frm 00020
Fmt 4702
Sfmt 4702
36555
Atmospheric Administration (NOAA),
Commerce.
ACTION:
Notice of public workshop.
SUMMARY: NMFS will present a
workshop on proposed catchmonitoring standards for the nonAmerican Fisheries Act (AFA) trawl
catcher/processor sector. These
standards are necessary to support
proposed groundfish and prohibited
species allocations to this sector that are
under consideration by the North
Pacific Fishery Management Council.
The workshop will be held
Monday, June 27, 2005, from 10 a.m. to
1 p.m.
DATES:
The workshop will be held
at the Nordby Center, located in
Fishermen’s terminal, 1711 W
Nickerson St, Seattle, WA.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Alan Kinsolving, 907–586–7228.
The North
Pacific Fisheries Management Council is
developing proposed Amendment 80 to
the Fishery Management Plan for
Groundfish of the Bering Sea and
Aleutian Islands Area (FMP).
Amendment 80 would allocate
prohibited species and target species
other than Pacific cod and pollock to
trawl catcher/processor vessels that are
not qualified to fish for pollock under
the AFA. One aspect of the analysis of
alternatives being developed for
Amendment 80 includes options for
catch monitoring, weighing, and
accounting standards for the non-AFA
trawl catcher/processor sector. NMFS is
conducting the June 27, 2005, workshop
so that interested industry members
may provide guidance to NMFS on the
development and implementation of
these standards.
This workshop is not intended to be
a forum for providing public comment
on the proposed rule to implement
proposed Amendment 79 to the FMP.
That proposed rule also would establish
catch monitoring standards for some
vessels within the non-AFA trawl
catcher/processor sector. Written
comments on Amendment 79 may be
submitted to NMFS consistent with the
protocol set forth in the preamble to the
proposed rule published in the Federal
Register on June 16, 2005 (70 FR 35054).
This workshop is physically
accessible to people with disabilities.
Requests for sign language
interpretation or other auxiliary aids
should be directed to Alan Kinsolving
(see FOR FURTHER INFORMATION CONTACT).
SUPPLEMENTARY INFORMATION:
E:\FR\FM\24JNP1.SGM
24JNP1
Agencies
[Federal Register Volume 70, Number 121 (Friday, June 24, 2005)]
[Proposed Rules]
[Pages 36554-36555]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-12481]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of Inspector General
45 CFR Part 61
RIN 0906-AA46
Office of the Secretary, Health Care Fraud and Abuse Data
Collection Program: Reporting of Final Adverse Actions; Correction
AGENCY: Office of Inspector General (OIG), HHS.
ACTION: Proposed correction amendment.
-----------------------------------------------------------------------
SUMMARY: This document proposes a correction to the final regulations,
which were published in the Federal Register on October 26, 1999 (64 FR
57740). These regulations established a national health care fraud and
abuse data collection program for the reporting and disclosing of
certain adverse actions taken against health care providers, suppliers
and practitioners, and for maintaining a data base of final adverse
actions taken against health care providers, suppliers and
practitioners. An inadvertent error appeared in the text of the
regulations concerning the definition of the term ``any other negative
action or finding.'' As a result, we are proposing to correct 45 CFR
61.3, Definitions, to assure the technical correctness of these
regulations.
DATES: To assure consideration, public comments must be mailed and
delivered to the address provided below by no later than 5 p.m., July
25, 2005.
ADDRESSES: Please mail or deliver your written comments to the
following address: Department of Health and Human Services, Office of
Inspector General, Attention: OIG-46-CA2, 330 Independence Avenue, SW.,
Room 5246, Washington, DC 20201.
FOR FURTHER INFORMATION CONTACT: Joel Schaer, OIG Regulations Officer
Office of External Affairs, (202) 619-0089.
SUPPLEMENTARY INFORMATION: The HHS Office of Inspector General (OIG)
issued final regulations on October 26, 1999 (64 FR 57740) that
established a national health care fraud and abuse data collection
program--the Healthcare Integrity and Protection Data Bank (HIPDB)--for
the reporting and disclosing of certain final adverse actions taken
against health care providers, suppliers and practitioners, and for
maintaining a data base of final adverse actions taken against health
care providers, suppliers and practitioners. The final rule established
a new 45 CFR part 61 to implement the requirements for reporting of
specific data elements to, and procedures for obtaining information
from, the HIPDB. In that final rule, an inadvertent error appeared in
Sec. 61.3--the definitions section of the regulations--and is now
being proposed for correction.
Section 61.3 expanded on previous regulatory definitions and
provided additional examples of the scope of various terms set fort in
the statute. On page 57755 of the preamble, summarizing the various
revisions being made to the final rule, we indicated that with respect
to the definition for the term ``any other negative action or finding''
there are certain kinds of actions or findings that would not meet the
intent of the statute and not be
[[Page 36555]]
reportable. We cited, as an example, administrative actions, such as
limited training permits, limited licenses for telemedicine, fines or
citations that do not restrict a practitioner's practice, or personnel
actions for tardiness, that were not within the range of actions
intended by the statute. As a result, we agreed to add a clarifying
phrase to this term. The revised definition would exclude
administrative fines or citations, corrective action plans and other
personnel actions, unless they are (1) connected to the billing,
provision or delivery of health care services, and (2) taken in
conjunction with other licensure or certification actions such as
revocation, suspension, censure, reprimand, probation, or surrender.
However, we inadvertently omitted this clarifying language to the
regulations text of the rule itself. Therefore, to be consistent with
the intended clarification and the overall intent of the final
rulemaking, we are correcting this inadvertent error in the definition
of the term ``any other negative action or finding'' that appeared on
page 57759 in the October 26, 1999 final regulations to include this
additional clarifying language.
Comments should be addressed specifically to the issue of
clarifying the existing definition of the term in question in
accordance with the earlier final rulemaking.
Response to Public Comments
Comments will be available for public inspection beginning on July
8, 2005 in Room 5518 of the Office of Inspector General at 330
Independence Avenue, SW., Washington DC, on Monday through Friday of
each week from 8 a.m. to 4 p.m., (202) 619-0089. Because of the number
of comments we normally receive on regulations, we will not acknowledge
or respond to them individually. However, we will consider all timely
and appropriate comments when developing the final corrections
amendment.
List of Subjects in 45 CFR Part 61
Billing and transportation services, Durable medical equipment
suppliers and manufacturers, Health care insurers, Health maintenance
organizations, Health professions, Home health care agencies,
Hospitals, Penalties, Pharmaceutical suppliers and manufacturers,
Privacy, Reporting and recordkeeping requirements, Skilled nursing
facilities.
Therefore, 45 CFR part 61 is proposed to be amended by making the
following correcting amendment:
PART 61--HEALTHCARE INTEGRITY AND PROTECTION DATA BANK FOR FINAL
ADVERSE INFORMATION ON HEALTH CARE PROVIDERS, SUPPLIERS AND
PRACTITIONERS
1. The authority citation for part 61 would continue to read as
follows:
Authority: 42 U.S.C. 1320a-7e.
2. Section 61.3 would be amended by republishing the introductory
text, and by revising the definition for the term ``Any other negative
action or finding'' to read as follows:
Sec. 61.3 Definitions.
The following definitions apply to this part:
* * * * *
Any other negative action or finding by a Federal or State
licensing agency means any action or finding that under the State's law
is publicly available information, and rendered by a licensing
authority, including but not limited to, limitations on the scope of
practice, liquidations, injunctions and forfeitures. This definition
also includes final adverse actions rendered by a Federal or State
licensing or certification authority, such as exclusions, revocations
or suspension of license or certification that occur in conjunction
with settlements in which no finding of liability has been made
(although such a settlement itself is not reportable under the
statute). This definition excludes administrative fines or citations
and corrective action plans and other personnel actions, unless they
are:
(1) Connected to the delivery of health care services; and
(2) taken in conjunction with other licensure or certification
actions such as revocation, suspension, censure, reprimand, probation
or surrender.
* * * * *
Dated: June 20, 2005.
Ann Agnew,
Executive Secretary to the Department.
[FR Doc. 05-12481 Filed 6-23-05; 8:45 am]
BILLING CODE 4152-01-P