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Guidance for Industry: Submitting and Reviewing Complete Responses to Clinical Holds

PRACRESPCM

OMB: 0910-0445

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DEPARTMENT OF HEALTH & HUMAN SERVICES

Food and Drug

Administration




Memorandum






Date


August 30, 2006


From





Director, Division of Management Systems, DMS

Paperwork Reduction Act and Records Management Branch, HFA-250




Subject




Request for OMB Approval of "Guidance for Industry Submitting and Reviewing Complete Responses to Clinical Holds”


To


Chief, Human Resources and Housing Branch

Office of Information and Regulatory Affairs, OMB

Through: Reports Clearance Officer, HHS_______



The purpose of this memorandum is to request OMB approval of the collection of information requirements for “Guidance for Industry Submitting and Reviewing Complete Responses to Clinical Holds.” The annual burden estimate imposed by this collection of information will be 51,120 hours.




Paul Jones




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