HIPAA Administrative Simplification: Standards for Electronic Health Care Claims Attachments; Extension of Comment Period, 70574-70575 [05-23077]
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70574
Federal Register / Vol. 70, No. 224 / Tuesday, November 22, 2005 / Proposed Rules
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Act (16 U.S.C. 6811).
Services, Department of Health and
Human Services, Attention: CMS–0050–
P, P.O. Box 8014, Baltimore, MD 21244–
8014.
Please allow sufficient time for mailed
comments to be received before the
close of the comment period.
3. By express or overnight mail. You
may send written comments (one
original and two copies) to the following
address ONLY: Centers for Medicare &
Medicaid Services, Department of
Health and Human Services, Attention:
CMS–0050–P, Mail Stop C4–26–05,
7500 Security Boulevard, Baltimore, MD
21244–1850.
4. By hand or courier. If you prefer,
you may deliver (by hand or courier)
your written comments (one original
and two copies) before the close of the
comment period to one of the following
addresses. If you intend to deliver your
comments to the Baltimore address,
please call telephone number (410) 786–
7195 in advance to schedule your
arrival with one of our staff members.
Room 445–G, Hubert H. Humphrey
Building, 200 Independence Avenue,
SW., Washington, DC 20201; or, 7500
Security Boulevard, Baltimore, MD
21244–1850.
(Because access to the interior of the
HHH Building is not readily available to
persons without Federal Government
identification, commenters are
encouraged to leave their comments in
the CMS drop slots located in the main
lobby of the building. A stamp-in clock
is available for persons wishing to retain
a proof of filing by stamping in and
retaining an extra copy of the comments
being filed.)
Comments mailed to the addresses
indicated as appropriate for hand or
courier delivery may be delayed and
received after the comment period.
For information on viewing public
comments, see the beginning of the
SUPPLEMENTARY INFORMATION section.
FOR FURTHER INFORMATION CONTACT:
Lorraine Doo, 410–786–6597.
Submitting Comments: We welcome
comments from the public on all issues
set forth in the September 23, 2005
proposed rule to assist us in fully
considering issues, developing policies
and adopting standards. You can assist
us by referencing the file code CMS–
0050–P and the specific ‘‘issue
identifier’’ that precedes the section on
which you choose to comment.
Inspection of Public Comments: All
comments received before the close of
the comment period are available for
viewing by the public, including any
personally identifiable or confidential
business information that is included in
a comment. CMS posts all comments
received before the close of the
comment period on its public Web site
as soon as possible after they have been
received. Comments received timely
will be available for public inspection as
they are received, generally beginning
approximately 3 weeks after publication
of a document, at the headquarters of
the Centers for Medicare & Medicaid
Services, 7500 Security Boulevard,
Baltimore, Maryland 21244, Monday
through Friday of each week from 8:30
a.m. to 4 p.m. To schedule an
appointment to view public comments,
phone 1–800–743–3951.
SUPPLEMENTARY INFORMATION: On
September 23, 2005, we published a
proposed rule in the Federal Register
(70 FR 55990) that would recommend
the adoption of a set of standards to
facilitate the electronic exchange of
clinical and administrative data to
further improve the claims adjudication
process when additional documentation
is required. This rule proposes two
X12N transaction standards: One to
request the information, and one to
respond to that request with the answer
or additional information. This rule also
proposes the use of Health Level 7 (HL7)
specifications for the content and format
of communicating the actual clinical
information. Finally, this rule proposes
the adoption of the Logical Observation
Identifiers, Names and Codes or
LOINC for specific identification of the
additional information being requested,
and the coded answers that respond to
the requests. Due to the highly technical
nature of the materials, and the size
(length) of the technical documents
being reviewed, we want to provide
additional time for the industry to
review and comment upon all of the
technical documents (implementation
guides, specifications, code sets,
modifiers), and the policies proposed in
the September 23, 2005 proposed rule.
Due to the complexity of this
proposed rule, the length of time
[FR Doc. 05–23113 Filed 11–21–05; 8:45 am]
BILLING CODE 4310–84–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
45 CFR Part 162
[CMS–0050–N]
RIN 0938–AK62
HIPAA Administrative Simplification:
Standards for Electronic Health Care
Claims Attachments; Extension of
Comment Period
Notice of extension of comment
period for proposed rule.
ACTION:
SUMMARY: This notice extends the
comment period for a proposed rule
published in the Federal Register on
September 23, 2005 (70 FR 55990) that
would recommend the adoption of a set
of standards to facilitate the electronic
exchange of clinical and administrative
data to further improve the claims
adjudication process when additional
documentation is required. Due to the
very technical nature of this rule, the
industry is asking for additional time to
conduct a more comprehensive and
thorough review in order to provide
comments to the Standards
Development Organizations as well as to
CMS. The comment period is extended
for 60 days.
DATES: The comment period is extended
to 5 p.m. on January 23, 2006.
ADDRESSES: In commenting, please refer
to file code CMS–0050–P. Because of
staff and resource limitations, we cannot
accept comments by facsimile (FAX)
transmission.
You may submit comments in one of
four ways (no duplicates, please):
1. Electronically. You may submit
electronic comments on specific issues
in the September 23, 2005 proposed rule
to https://www.cms.hhs.gov/regulations/
ecomments. (Attachments should be in
Microsoft Word, WordPerfect, or Excel;
however, we prefer Microsoft Word.)
2. By regular mail. You may mail
written comments (one original and two
copies) to the following address ONLY:
Centers for Medicare & Medicaid
VerDate Aug<31>2005
18:06 Nov 21, 2005
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22NOP1
Federal Register / Vol. 70, No. 224 / Tuesday, November 22, 2005 / Proposed Rules
between the development of the
proposed standards and the publication
of this proposed rule, the potential need
to upgrade the data content of the
specifications or the use of Release 2 of
the Clinical Document Architecture
(CDA), numerous members of the
industry and professional associations
have requested more time to analyze the
potential impact and consequences of
the proposed rule. Thus, we have
decided to extend the comment period
for an additional 60 days. This
document announces the extension of
the public comment period to January
23, 2006.
Authority: Secs. 1173 and 1175 of the
Social Security Act (42 U.S.C. 1302d–2 and
1320d–4).
Dated: November 9, 2005.
Mark B. McClellan,
Administrator, Centers for Medicare &
Medicaid Services.
Dated: November 17, 2005.
Michael O. Leavitt,
Secretary.
[FR Doc. 05–23077 Filed 11–21–05; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
50 CFR Part 622
[Docket No. 051114298–5298–01; I.D.
110105C]
RIN 0648–AT12
Fisheries of the Caribbean, Gulf of
Mexico, and South Atlantic; Gulf of
Mexico Commercial Grouper Fishery;
Trip Limit
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Proposed rule; request for
comments.
AGENCY:
SUMMARY: NMFS issues this proposed
rule to implement a regulatory
amendment to the Fishery Management
Plan for the Reef Fish Resources of the
Gulf of Mexico (FMP) prepared by the
Gulf of Mexico Fishery Management
Council (Council). This proposed rule
would establish a 6,000–lb (2,722–kg)
commercial trip limit for shallow-water
and deep-water grouper, combined, in
the exclusive economic zone of the Gulf
of Mexico. The intended effect of this
proposed rule is to minimize the effects
of derby fishing and prolong the fishing
season.
VerDate Aug<31>2005
19:26 Nov 21, 2005
Jkt 208001
Written comments on the
proposed rule must be received no later
than 5 p.m., eastern time, on December
7, 2005.
ADDRESSES: You may submit comments
on the proposed rule by any of the
following methods:
• E-mail: 0648–
AT12.Proposed@noaa.gov. Include in
the subject line the following document
identifier: 0648–AT12.
• Federal e-Rulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Andy Strelcheck, Southeast
Regional Office, NMFS, 263 13th
Avenue South, St. Petersburg, FL 33701.
• Fax: 727–824–5308; Attention: Andy
Strelcheck.
Copies of the regulatory amendment,
which includes a Regulatory Impact
Review (RIR), an Initial Regulatory
Flexibility Analysis (IRFA), and an
Environmental Assessment (EA), may be
obtained from the Gulf of Mexico
Fishery Management Council, 2203 N.
Lois Avenue, Suite 1100, Tampa, FL
33607; telephone: 813–348–1630; fax:
813–348–1711; e-mail:
gulfcouncil@gulfcouncil.org. Copies of
the regulatory amendment may also be
downloaded from the Council’s website
at www.gulfcouncil.org.
FOR FURTHER INFORMATION CONTACT:
Andy Strelcheck, telephone: 727–824–
5374; fax: 727–824–5308; e-mail:
andy.stelcheck@noaa.gov.
SUPPLEMENTARY INFORMATION: The reef
fish fishery of the Gulf of Mexico is
managed under the FMP. The FMP was
prepared by the Council and is
implemented under the authority of the
Magnuson-Stevens Fishery
Conservation and Management Act
(Magnuson-Stevens Act) by regulations
at 50 CFR part 622.
On July 15, 2004 (69 FR 33315, June
15, 2004), NMFS implemented
Secretarial Amendment 1 to the FMP to
establish a red grouper rebuilding plan,
including a 5.31 million-lb (2.42
million-kg), gutted weight, commercial
quota and a 1.25 million-lb (0.57
million-kg), gutted weight, recreational
target catch level for red grouper.
Secretarial Amendment 1 also reduced
the commercial quotas for deep-water
grouper (i.e., speckled hind and
yellowedge, misty, warsaw, and snowy
grouper) and shallow-water grouper
(i.e., all grouper other than deep-water
grouper, goliath grouper, and Nassau
grouper and including scamp before the
quota for shallow-water grouper is
reached). In 2004, the commercial deepwater grouper and shallow-water
grouper quotas were reached prior to the
end of the fishing year, and the fisheries
DATES:
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70575
were closed on July 15, 2004 (69 FR
41433, July 9, 2004), and November 15,
2004 (69 FR 65092, November 10, 2004),
respectively. In November 2004, the
Council, at the request of
representatives of the commercial
grouper fishing industry, asked NMFS
to develop an emergency or interim rule
establishing trip limits for the
commercial grouper fishery in 2005.
Trip limits, which began at 10,000 lb
(4,536 kg) and stepped down to 7,500 lb
(3,402 kg) and then to 5,500 lb (2,495
kg) at defined trigger points, were
implemented by NMFS through an
emergency rule that was effective from
March 3 through August 16, 2005 (70 FR
8037, February 17, 2005). NMFS
extended the emergency rule and trip
limits for an additional 180 days
effective August 17, 2005, through
February 12, 2006 (70 FR 48323, August
17, 2005). These trip limits were
implemented to prolong the shallowwater grouper and deep-water grouper
fishing seasons in 2005 and to reduce
the adverse effects associated with
derby fishing. However, the emergency
trip limits were not restrictive enough to
achieve the intended objectives. In fact,
the deep-water and shallow-water
grouper fisheries closed earlier in 2005
(June 23, 2005, and October 10, 2005,
respectively) than they had in 2004.
The Council prepared a regulatory
amendment to evaluate alternatives and
establish more permanent trip limits for
the commercial grouper fishery. After
considering the effectiveness of existing
trip limits, management alternatives,
and public testimony, the Council
adopted a 6,000–lb (2,722–kg)
commercial trip limit for shallow-water
grouper and deep-water grouper,
combined. This proposed rule would
implement the 6,000–lb (2,722–kg) trip
limit. To maximize the effectiveness of
this more restrictive trip limit, the
Council and NMFS have agreed the
existing trip limits implemented via
emergency rule (70 FR 48323, August
17, 2005) would terminate upon
implementation of the 6,000–lb (2,722–
kg) trip limit proposed in this rule.
Classification
NMFS has determined that the
proposed rule is consistent with the
FMP and preliminarily determined that
the rule is consistent with the
Magnuson-Stevens Fishery
Conservation and Management Act and
other applicable laws.
This proposed rule has been
determined to be not significant for
purposes of Executive Order 12866.
NMFS prepared an IRFA as required
by section 603 of the Regulatory
Flexibility Act. The IRFA describes the
E:\FR\FM\22NOP1.SGM
22NOP1
Agencies
[Federal Register Volume 70, Number 224 (Tuesday, November 22, 2005)]
[Proposed Rules]
[Pages 70574-70575]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-23077]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Secretary
45 CFR Part 162
[CMS-0050-N]
RIN 0938-AK62
HIPAA Administrative Simplification: Standards for Electronic
Health Care Claims Attachments; Extension of Comment Period
ACTION: Notice of extension of comment period for proposed rule.
-----------------------------------------------------------------------
SUMMARY: This notice extends the comment period for a proposed rule
published in the Federal Register on September 23, 2005 (70 FR 55990)
that would recommend the adoption of a set of standards to facilitate
the electronic exchange of clinical and administrative data to further
improve the claims adjudication process when additional documentation
is required. Due to the very technical nature of this rule, the
industry is asking for additional time to conduct a more comprehensive
and thorough review in order to provide comments to the Standards
Development Organizations as well as to CMS. The comment period is
extended for 60 days.
DATES: The comment period is extended to 5 p.m. on January 23, 2006.
ADDRESSES: In commenting, please refer to file code CMS-0050-P. Because
of staff and resource limitations, we cannot accept comments by
facsimile (FAX) transmission.
You may submit comments in one of four ways (no duplicates,
please):
1. Electronically. You may submit electronic comments on specific
issues in the September 23, 2005 proposed rule to https://
www.cms.hhs.gov/regulations/ecomments. (Attachments should be in
Microsoft Word, WordPerfect, or Excel; however, we prefer Microsoft
Word.)
2. By regular mail. You may mail written comments (one original and
two copies) to the following address ONLY: Centers for Medicare &
Medicaid Services, Department of Health and Human Services, Attention:
CMS-0050-P, P.O. Box 8014, Baltimore, MD 21244-8014.
Please allow sufficient time for mailed comments to be received
before the close of the comment period.
3. By express or overnight mail. You may send written comments (one
original and two copies) to the following address ONLY: Centers for
Medicare & Medicaid Services, Department of Health and Human Services,
Attention: CMS-0050-P, Mail Stop C4-26-05, 7500 Security Boulevard,
Baltimore, MD 21244-1850.
4. By hand or courier. If you prefer, you may deliver (by hand or
courier) your written comments (one original and two copies) before the
close of the comment period to one of the following addresses. If you
intend to deliver your comments to the Baltimore address, please call
telephone number (410) 786-7195 in advance to schedule your arrival
with one of our staff members. Room 445-G, Hubert H. Humphrey Building,
200 Independence Avenue, SW., Washington, DC 20201; or, 7500 Security
Boulevard, Baltimore, MD 21244-1850.
(Because access to the interior of the HHH Building is not readily
available to persons without Federal Government identification,
commenters are encouraged to leave their comments in the CMS drop slots
located in the main lobby of the building. A stamp-in clock is
available for persons wishing to retain a proof of filing by stamping
in and retaining an extra copy of the comments being filed.)
Comments mailed to the addresses indicated as appropriate for hand
or courier delivery may be delayed and received after the comment
period.
For information on viewing public comments, see the beginning of
the SUPPLEMENTARY INFORMATION section.
FOR FURTHER INFORMATION CONTACT: Lorraine Doo, 410-786-6597.
Submitting Comments: We welcome comments from the public on all
issues set forth in the September 23, 2005 proposed rule to assist us
in fully considering issues, developing policies and adopting
standards. You can assist us by referencing the file code CMS-0050-P
and the specific ``issue identifier'' that precedes the section on
which you choose to comment.
Inspection of Public Comments: All comments received before the
close of the comment period are available for viewing by the public,
including any personally identifiable or confidential business
information that is included in a comment. CMS posts all comments
received before the close of the comment period on its public Web site
as soon as possible after they have been received. Comments received
timely will be available for public inspection as they are received,
generally beginning approximately 3 weeks after publication of a
document, at the headquarters of the Centers for Medicare & Medicaid
Services, 7500 Security Boulevard, Baltimore, Maryland 21244, Monday
through Friday of each week from 8:30 a.m. to 4 p.m. To schedule an
appointment to view public comments, phone 1-800-743-3951.
SUPPLEMENTARY INFORMATION: On September 23, 2005, we published a
proposed rule in the Federal Register (70 FR 55990) that would
recommend the adoption of a set of standards to facilitate the
electronic exchange of clinical and administrative data to further
improve the claims adjudication process when additional documentation
is required. This rule proposes two X12N transaction standards: One to
request the information, and one to respond to that request with the
answer or additional information. This rule also proposes the use of
Health Level 7 (HL7) specifications for the content and format of
communicating the actual clinical information. Finally, this rule
proposes the adoption of the Logical Observation Identifiers, Names and
Codes or LOINC[supreg] for specific identification of the additional
information being requested, and the coded answers that respond to the
requests. Due to the highly technical nature of the materials, and the
size (length) of the technical documents being reviewed, we want to
provide additional time for the industry to review and comment upon all
of the technical documents (implementation guides, specifications, code
sets, modifiers), and the policies proposed in the September 23, 2005
proposed rule.
Due to the complexity of this proposed rule, the length of time
[[Page 70575]]
between the development of the proposed standards and the publication
of this proposed rule, the potential need to upgrade the data content
of the specifications or the use of Release 2 of the Clinical Document
Architecture (CDA), numerous members of the industry and professional
associations have requested more time to analyze the potential impact
and consequences of the proposed rule. Thus, we have decided to extend
the comment period for an additional 60 days. This document announces
the extension of the public comment period to January 23, 2006.
Authority: Secs. 1173 and 1175 of the Social Security Act (42
U.S.C. 1302d-2 and 1320d-4).
Dated: November 9, 2005.
Mark B. McClellan,
Administrator, Centers for Medicare & Medicaid Services.
Dated: November 17, 2005.
Michael O. Leavitt,
Secretary.
[FR Doc. 05-23077 Filed 11-21-05; 8:45 am]
BILLING CODE 4120-01-P