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本帖最后由 beiwei5du 于 2015-4-3 23:13 编辑
New FDAAnimal Drug Product Guidance Now Available 新的FDA动物药品行业指南现发布 4. 2, 2015 The United States Pharmacopeia requiresthe control of residual solvents in drug products marketed within this country.Because the animaldrug products the FDA regulates are administered to many diverse animal species, the agency allowsfor a flexible approachto implementing the USP requirements governing residual solvents. Guidance documents represent the FDA’slatest thinking on particular topics, policies and regulatory issues. While guidancedocuments are prepared primarily for the benefit of industry, they also areused by FDA staff and other stakeholders to understand the agency’sinterpretation of regulations and policies. The FDA is accepting public commentsbeginning on Friday, April 3, 2015. To electronically submit comments to thedocket, visit www.regulations.gov andtype FDA-2010-D-0566 in the search box. To submit comments to the docket bymail, use the following address. Be sure to include docket numberFDA-2010-D-0566 on each page of your written comments. Division of Dockets Management
HFA-305
Food and Drug Administration
5630 Fishers Lane, Room 1061
Rockville, MD 20852
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发表于 2015-4-3 23:06:20
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