[Federal Register Volume 60, Number 97 (Friday, May 19, 1995)]
[Notices]
[Pages 26892-26893]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-12256]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Public Health Service
Agency Forms Undergoing Paperwork Reduction Act Review
Each Friday the Public Health Service (PHS) publishes a list of
information collection requests under review, in compliance with the
Paperwork Reduction Act (44 U.S.C. Chapter 35). To request a copy of
these requests, call the PHS Reports Clearance Office on (202) 690-
7100.
The following requests have been submitted for review since the
list was last published on May 12.
1. Studies of Adverse Reproductive Outcomes in Female Occupational
Groups--New--The reproductive health of a group of female workers
exposed to a particular environmental chemical agent will be compared
to the reproductive health of a group of working women with no
occupational exposure to known or suspected reproductive toxicants.
Respondents: Individuals or households; Business or other for-profit.
Send comments to Shannah Koss, Human Resources and Housing Branch, New
Executive Office Building, Room 10235, Washington, DC 20503.
[[Page 26893]]
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No. of
No. of responses Avg. burden/
respondents per response
respondent
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Women........................ 6,200 1 2.85 hours.
Physicians................... 1,200 1 .5 hour.
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Estimated Annual Burden: 18,250 hours.
2. Infant Feeding Study Puberty Follow-up--0925-0381--Extension, no
change--Children from a previous study of health effects of PCBs and
DDE are being restudied to determine whether PCBs or DDE affect growth
or pubertal development. Information is being collected annually from
431 children and their parents to determine whether there is public
health concern about these chemicals in children. Respondents:
Individuals or households; Number of Respondents: 862; Number of
Responses per Respondent: 1.1; Average Burden per Response: 0.23 hour;
Estimated Annual Burden: 219 hours. Send comments to James Scanlon,
Office of the Assistant Secretary for Health, Room 737-F, Humphrey
Building, 200 Independence Ave., SW., Washington, DC 20201.
3. FDA Recall Regulations--0910-0249--Extension, no change--Recall
guidelines set forth procedures to be used by manufacturers and
distributors or other responsible persons in notifying or alerting
health professionals or other persons of an unreasonable risk of
substantial harm to the public's health and describe the procedures
used or required by FDA in the recall process. Respondents: Business or
other for-profit. Send comments to Shannah Koss, Human Resources and
Housing Branch, New Executive Office Building, Room 10235, Washington,
DC 20503.
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No. of
No. of responses/ Avg. burden/
respondents respondents response
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21 CFR 7.42................... 1,294 1 1.8 hours.
21 CFR 7.46/7.49.............. 1,294 1 4 hours.
21 CFR 7.53................... 1,294 1 36 hours.
21 CFR 7.55(b)................ 1,294 1 2 hours.
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Estimated Annual Burden: 56,677 hours.
Written Comments and recommendations concerning the proposed
information collections should be sent within 30 days of this notice
directly to the individual designated.
Dated: May 12, 1995.
James Scanlon,
Director, Data Policy Staff, Office of the Assistant Secretary for
Health and PHS Report Clearance Officer.
[FR Doc. 95-12256 Filed 5-18-95; 8:45 am]
BILLING CODE 4160-01-M
