LABORATORY STUDIES FOR THE APPROVAL OF AQUACULTURE DRUGS

K. Greenlees
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引用次数: 22

Abstract

Abstract All drugs approved by the U.S. Food and Drug Administration (FDA) must be shown to be safe and efficacious. The data required to demonstrate the safety and efficacy of a new animal drug are typically produced through controlled studies conducted by pharmaceutical firms that invest considerable time and money into the process. Factors that have contributed to the paucity of approved drugs for U.S. aquaculture include the relatively limited market for aquaculture drugs and the difficulty involved in conducting studies traditionally carried out in the drug approval process in an aquatic environment. One approach to this problem has been the development of data from other sources. In recent years, government, academic, and private researchers have conducted studies in an attempt to produce the data necessary to satisfy the requirements for the approval of new animal drugs in aquaculture. The data may then be made publicly available and can be used by a sponsor of the drug product to satisfy part of t...
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批准水产养殖药物的实验室研究
美国食品和药物管理局(FDA)批准的所有药物都必须证明是安全有效的。证明一种新的动物药物的安全性和有效性所需的数据通常是通过制药公司进行的对照研究产生的,制药公司在这一过程中投入了大量时间和金钱。导致美国水产养殖批准药物稀少的因素包括水产养殖药物的市场相对有限,以及在水生环境中进行传统的药物批准过程中进行的研究所涉及的困难。解决这个问题的一种方法是从其他来源获取数据。近年来,政府、学术界和私人研究人员进行了研究,试图提供必要的数据,以满足批准水产养殖中新的动物药物的要求。然后,这些数据可以公开提供,并且可以由药品的赞助商使用,以满足部分…
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