[Federal Register: December 6, 2004 (Volume 69, Number 233)]
[Notices]
[Page 70458]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr06de04-41]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 2004N-0395]
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.
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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 January
5, 2005.
ADDRESSES: OMB is still experiencing significant delays in the regular
mail, including first class and express mail, and messenger deliveries
are not being accepted. To ensure that comments on the information
collection are received, OMB recommends that comments be faxed to the
Office of Information and Regulatory Affairs, OMB, Attn: Fumie Yokota,
Desk Officer for FDA, FAX: 202-395-6974.
FOR FURTHER INFORMATION CONTACT: Peggy Robbins, Office of Management
Programs (HFA-250), Food and Drug Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301-827-1223.
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
Collecting applications for the Medical Device Fellowship Plan 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 September 20, 2004 (69 FR 56228), FDA
published a 60-day notice requesting public comment on the information
collection provisions. No comments were received.
FDA estimates the burden of this collection of information as
follows:
Table 1-Estimated Annual Reporting Burden\1\
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No. of Annual Frequency Total Annual Hours per
FDA Form No. Respondents per Response Responses Response Total Hours
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FDA Form 3608 100 1 100 1 100
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\1\ There are no capital costs or operating and maintenance costs associated with this collection of
information.
FDA based these estimates on the number of inquiries that have been
received about the program and requests for application forms over the
past year. We anticipate the number of interested individuals and
universities, and subsequent number of applications, to increase as we
continue to develop an outreach program and an alumni base.
In addition, we would expect applicants who are not selected for
their preferred term of employment to reapply at a later date. For
these reasons we would expect that the number of applications submitted
in the second and third years would increase substantially. During the
first year, we expect to receive 100 applications. We believe that we
will receive approximately 100 applications the second year and 100
applications the third year. FDA believes it will take individuals 1
hour to complete the application. This is based on similar applications
submitted to FDA.
Dated: November 26, 2004.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. 04-26672 Filed 12-3-04; 8:45 am]
BILLING CODE 4160-01-S