历史与当代视野下的国际生物标准化。

M R Hilleman
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引用次数: 0

摘要

重新叙述培育和控制新的和现有的生物产品的概念和制度的起源和发展是历史回顾的一个肥沃的主题。它描述了什么是必要的和功能性的活动,需要付诸实施。生物制品监管最早的例子是由18世纪的发明家自己创造的,并在过去的一个世纪里,随着国家监管机构的建立,这些机构的数量和复杂性不断增加,逐渐制度化。1948年,世界卫生组织(世卫组织)成立,并制定了生物标准和条例,作为对成员国的咨询。这也变得越来越复杂,现在在世界范围内的生物制品企业中至关重要。生物标准化和管制领域可以从其促进技术发展的需要和作用以及确保这项努力的成果值得和得到保留的角度来看待。在许多方面,这是一个关于麻烦、悲剧和胜利的故事,这些在文本中都有叙述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
International biological standardization in historic and contemporary perspective.

Recounting the origination and development of the concepts and institutions to foster and control new and existing biological products is a fertile subject for historical review. It describes what was a necessary and functional activity that needed to be brought into being. The earliest examples of biologicals regulation were created by the eighteenth century inventors themselves and became progressively institutionalized by the creation of national control authorities which increased in number and sophistication during the past century. In 1948, the World Health Organization (WHO) was established and created biological standards and regulations as an advisory to member nations. This too has grown in sophistication and is now of central importance in the biologicals enterprise worldwide. The field of biological standardization and regulation can be viewed in its need and role to foster technological development and to assure that the products of that endeavour are worthy and are retained. In many respects, it is a tale of troubles, tragedies, and triumphs and this is recounted in the text.

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