美国农业部兽医生物制品管理条例。使用许可前评估和许可后监测来实现法规遵从。

R E Hill, D C Randall
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引用次数: 0

摘要

美国农业部负责管理美国的兽医生物产品,1913年《动物病毒-血清-毒素法》规定了监管权力。该法案授权农业部长颁布进入美国、在美国境内或从美国出口的兽医生物制品的生产、测试和销售条例。目前的监管计划包括对产品、标签、设施和人员进行广泛的许可前审查,以及许可后监测系统的不事先通知的深入检查,产品批次(系列)的上市前控制,成品的随机检查测试和上市后流行病学监测。这种许可前后的监管结合确保了纯、安全、强效和有效的兽医生物制剂可在美国使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Unites States Department of Agriculture Regulation of Veterinary Biological Products. The use of prelicensing evaluation and postlicensing monitoring to achieve regulatory compliance.

The United Stated Department of Agriculture is responsible for regulating veterinary biological products in the United States, and the regulatory authority is provided in the Animal Virus-serum-Toxin Act of 1913. The act authorizes the Secretary of Agriculture to promulgate regulations for the production, testing, and marketing of veterinary biological products into, within, or from the United States. The current regulatory program consists of extensive prelicensing review of products, labeling, facilities, and personnel and a postlicensing monitoring system of unannounced in-depth inspections, premarketing control of product batches (serials), random check testing of finished product, and postmarketing epidemiological surveillance. This combination of regulatory oversight before and after licensure assures that pure, safe, potent, and effective veterinary biologics are available for use in the United States.

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