Agency Information Collection Activities; Proposals, Submissions, and Approvals:
Federal Register: January 27, 2011 (Volume 76, Number 18)
Notices
Page 4913-4914
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
DOCID:fr27ja11-75
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
Docket No. FDA-2010-N-0544
Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Application for
Participation in the Medical Device Fellowship Program
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
SUMMARY: The Food and Drug Administration (FDA) is announcing that a proposed collection of information has been submitted to the Office of
Management and Budget (OMB) for review and clearance under the
Paperwork Reduction Act of 1995.
DATES: Fax written comments on the collection of information by
February 28, 2011.
ADDRESSES: To ensure that comments on the information collection are received, OMB recommends that written comments be faxed to the Office of Information and Regulatory Affairs, OMB, Attn: FDA Desk Officer,
FAX: 202-395-7285, or emailed to oira_submission@omb.eop.gov. All comments should be identified with the OMB control number 0910-0551.
Also include the FDA docket number found in brackets in the heading of this document.
FOR FURTHER INFORMATION CONTACT: Daniel Gittleson, Office of
Information Management, Food and Drug Administration, 1350 Piccard Dr.,
PI50-400B, Rockville, MD 20850, 301-796-5156,
Daniel.Gittleson@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, FDA has submitted the following proposed collection of information to OMB for review and clearance.
Application for Participation in the Medical Device Fellowship
Program--(OMB Control Number 0910-0551)--Extension
Sections 1104, 1302, 3301, 3304, 3320, 3361, 3393, and 3394 of
Title 5 of the United States Code authorize Federal Agencies to rate applicants for Federal jobs. Collecting applications for the Medical
Device Fellowship Program will allow FDA's Center for Devices and
Radiological Health (CDRH) to easily and efficiently elicit and review information from students and health care professionals who are interested in becoming involved in CDRH activities. The process will reduce the time and cost of submitting written documentation to the
Agency and lessen the likelihood of applications being misrouted within the Agency mail system. It will assist the Agency in promoting and protecting the public health by encouraging outside persons to share their expertise with CDRH.
In the Federal Register of October 27, 2010 (75 FR 66103), FDA published a 60-day notice requesting public comment on the proposed collection of information. No comments were received.
FDA estimates the burden of this collection of information as follows:
Table 1--Estimated Annual Reporting Burden \1\
Number of
Annual frequency
Total annual
Hours per 5 U.S.C. Section
FDA Form No.
respondents
per response
responses
response
Total hours
1104, 1302, 3301, 3304, 3320, 3361, 3393,
3608
250
1
250
1
250 3394.......................................
\1\ There are no capital costs or operating and maintenance costs associated with this collection of information.
Page 4914
FDA based these estimates on the number of inquiries that have been received concerning the program and the number of requests for application forms over the past 3 years.
Dated: January 19, 2011.
Leslie Kux,
Acting Assistant Commissioner for Policy.
FR Doc. 2011-1760 Filed 1-26-11; 8:45 am
BILLING CODE 4160-01-P