[Federal Register: July 14, 2006 (Volume 71, Number 135)]
[Notices]
[Page 40126-40127]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr14jy06-92]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10205]
Emergency Clearance: Public Information Collection Requirements
Submitted to the Office of Management and Budget (OMB)
AGENCY: Center for Medicare & Medicaid Services, HHS.
In compliance with the requirement of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Centers for Medicare & Medicaid
Services (CMS), Department of Health and Human Services, is publishing
the following summary of proposed collections for public comment.
Interested persons are invited to send comments regarding this burden
estimate or any other aspect of this collection of information,
including any of the following subjects: (1) The necessity and utility
of the proposed information collection for the proper performance of
the agency's functions; (2) the accuracy of the estimated burden; (3)
ways to enhance the quality, utility, and clarity of the information to
be collected; and (4) the use of automated collection techniques or
[[Page 40127]]
other forms of information technology to minimize the information
collection burden.
We are, however, requesting an emergency review of the information
collection referenced below. In compliance with the requirement of
section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, we have
submitted to the Office of Management and Budget (OMB) the following
requirements for emergency review. We are requesting an emergency
review because the collection of this information is needed before the
expiration of the normal time limits under OMB's regulations at 5 CFR
part 1320. If these events do not occur according to the statutorily
mandated timeline, other statutory requirements will not be able to be
met. Section 6001(c) of the Deficit Reduction Act of 2005 (DRA)
requires CMS and the Office of Inspector General to analyze and, if
appropriate, redefine the Average Manufacturer Price (AMP). We have
determined that this information collection is needed because we do not
currently collect the necessary data needed to perform the AMP data
analysis as mandated by the DRA.
1. Type of Information Collection Request: New collection; Title of
Information Collection: Voluntary Sample Average Manufacturer Price
(AMP) Collection; Use: Section 1927 of the Social Security Act requires
each participating drug manufacturer to report quarterly product and
pricing information to CMS. The DRA modified parts of Section 1927 to
require that AMP be analyzed and redefined; Form Number: CMS-10205
(OMB: 0938-NEW); Frequency: Reporting--As needed; Affected
Public: Business or other for-profit; Number of Respondents: 550; Total
Annual Responses: 550; Total Annual Hours: 11,000.
CMS is requesting OMB review and approval of this collection by
July 31, 2006, with a 180-day approval period. Written comments and
recommendation will be considered from the public if received by the
individuals designated below by July 29, 2006.
To obtain copies of the supporting statement and any related forms
for the proposed paperwork collections referenced above, access CMS'
Web Site address at http://www.cms.hhs.gov/regulations/pra or E-mail
your request, including your address, phone number, OMB number, and CMS
document identifier, to Paperwork@cms.hhs.gov, or call the Reports
Clearance Office on (410) 786-1326.
Interested persons are invited to send comments regarding the
burden or any other aspect of these collections of information
requirements. However, as noted above, comments on these information
collection and recordkeeping requirements must be mailed and/or faxed
to the designees referenced below by July 29, 2006:
CMS, Office of Strategic Operations and Regulatory Affairs, Division of
Regulations Development--A, Attn: Melissa Musotto (CMS-10205), Room C4-
26-05, 7500 Security Boulevard, Baltimore, MD 21244-1850
and,
OMB Human Resources and Housing Branch, Attention: Katherine Astrich,
New Executive Office Building, Room 10235, Washington, DC 20503. Fax
Number: (202) 395-6974.
Dated: July 10, 2006.
Michelle Shortt,
Director, Regulations Development Group, Office of Strategic Operations
and Regulatory Affairs.
[FR Doc. 06-6191 Filed 7-10-06; 1:18 pm]
BILLING CODE 4120-01-P