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美国农业部目前对生物技术衍生兽用生物制品的许可程序。

Current USDA procedures for licensing biotechnology-derived veterinary biologicals.

作者信息

Gay C G

机构信息

USDA/APHIS/BBEP, Hyattsville, MD 20782.

出版信息

Dev Biol Stand. 1992;79:65-74.

PMID:1286767
Abstract

The establishment of appropriate procedures for regulating the commercialization of biotechnology products is an international issue which has been debated extensively in many countries. This paper will discuss the current procedures that have been established for the regulation of biotechnology-derived veterinary biologicals within the United States Department of Agriculture (USDA) and more specifically within Biotechnology, Biologics, and Environmental Protection (BBEP) of the Animal and Plant Health Inspection Service (APHIS). These procedures implement recent BBEP regulatory policy that has been developed to ensure risk-based regulation and avoid excessive restrictions that might curtail the development of biotechnology products.

摘要

建立适当的程序来规范生物技术产品的商业化是一个国际问题,在许多国家都进行了广泛的辩论。本文将讨论美国农业部(USDA)内,更具体地说是动植物卫生检验局(APHIS)的生物技术、生物制品和环境保护处(BBEP)内,目前已建立的用于监管生物技术衍生兽用生物制品的程序。这些程序实施了BBEP最近制定的监管政策,该政策旨在确保基于风险的监管,并避免可能限制生物技术产品开发的过度限制。

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