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75 FR 54589 - Availability of an Environmental Assessment for Field Testing Foot-and-Mouth Disease Vaccine, Live Adenovirus Vector

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Publication TitleMouse over help for Publication Title says The title of the publication. Individual Federal Register documents can be searched using the title field operator. Search field operator example is title:california volume:73 issue:25. Federal Register Volume 75, Issue 173 (September 8, 2010)
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GS 4.107:
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DatesMouse over help for Dates says Full text field which identifies the dates important to the regulation, such as the effective date, deadlines for comments, etc. Search field operator example is dates:effective.We will consider all comments that we receive on or before October 8, 2010.
ContactMouse over help for Contact says Contact information for more information about the notice or rule. Search field operator example is contact:fax.Dr. Albert P. Morgan, Section Leader, Operational Support Section, Center for Veterinary Biologics, Policy, Evaluation, and Licensing, VS, APHIS, 4700 River Road Unit 148, Riverdale, MD 20737-1231; phone (301) 734-8245, fax (301) 734-4314.
SummaryMouse over help for Summary says Summary of the rule or notice. Search field operator example is summary:airworthiness.We are advising the public that the Animal and Plant Health Inspection Service has prepared an environmental assessment (EA) concerning authorization to ship for the purpose of field testing, and then to field test, an unlicensed foot-and-mouth disease vaccine, live adenovirus vector. The EA, which is based on a risk analysis prepared to assess the risks associated with the field testing of this vaccine, examines the potential effects that field testing this veterinary vaccine could have on the quality of the human environment. Based on the risk analysis, we have reached a preliminary determination that field testing this veterinary vaccine will not have a significant impact on the quality of the human environment, and that an environmental impact statement need not be prepared. We intend to authorize shipment of this vaccine for field testing following the close of the comment period for this notice unless new substantial issues bearing on the effects of this action are brought to our attention. We also intend to issue a U.S. Veterinary Biological Product license for this vaccine, provided the field test data support the conclusions of the EA and the issuance of a finding of no significant impact and the product meets all other requirements for licensing.
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Animal and Plant Health Inspection Service
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Document in Context
This is part of Federal Register Volume 75, Issue 173 (September 8, 2010)
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