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【维基解密】fda101810
4160-01-P
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2009–D–0568]
Agency Information Collection Activities; Submission for Office of Management and
Budget Review; Comment Request; Draft Guidance for Industry on Planning for the Effects
of High Absenteeism to Ensure Availability of Medically Necessary Drug Products
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 [INSERT DATE 30
DAYS AFTER DATE OF PUBLICATION IN THE FEDERAL REGISTER].
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 e-mailed to
oira_submission@omb.eop.gov. All comments should be identified with the OMB control
number 0910-NEW and title Draft Guidance for Industry on Planning for the Effects of
High Absenteeism to Ensure Availability of Medically Necessary Drug Products (MNPs).
Also include the FDA docket number found in brackets in the heading of this document.
FOR FURTHER INFORMATION CONTACT:
Elizabeth Berbakos,
Office of Information Management,
2
Food and Drug Administration,
1350 Piccard Dr.,
PI50-400Q,
Rockville, MD 20850,
301-796-7392,
Elizabeth.berbakos@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.
Draft Guidan
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