Regulatory Perspectives : Where We Came from, Where Are We Today, Where Are We Headed?

C. Peck
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Abstract

While frequent employment of the phrase “regulatory science” by regulators and academics arose within the last three decades, “science” applied to “regulation” of medicinals dates back many centuries. Descriptive science characterized the earliest classifications of medicinal substances, employed for self-regulation by apothecaries and physicians. Later, development of chemical and biological techniques permitted more precise descriptions of biological and drug products, which were adaptable to development of quantitative product specifications for governmental regulation of manufacturers. Motivated by need to protect and support public health, advanced regulatory science has been applied to research regulatory standards and requirements. Advanced regulatory science is currently being researched and intensively applied in both medical product regulation and development. Ever more novel regulatory science is likely to contribute in a crucial way to undreamed of advances in pharmaceutical development and improved public health.
监管视角:我们从哪里来,我们今天在哪里,我们将向哪里去?
虽然监管者和学者在过去三十年中频繁使用“监管科学”一词,但将“科学”应用于药物“监管”可以追溯到许多世纪以前。描述科学以最早的药物分类为特征,用于药剂师和医生的自我调节。后来,化学和生物技术的发展使得对生物和药物产品的描述更加精确,这适应了政府对制造商进行监管的定量产品规格的发展。出于保护和支持公众健康的需要,先进的监管科学已被应用于研究监管标准和要求。目前正在研究先进的监管科学,并将其广泛应用于医疗产品的监管和开发。越来越多的新监管科学可能以一种至关重要的方式,为制药开发和改善公共卫生方面意想不到的进步做出贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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