波兰临床试验的法律问题

Katarzyna Syroka-Marczewska
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引用次数: 0

摘要

临床试验是在人体中进行的每一项试验,目的是发现或确认一种或多种临床研究药品的临床、药理学(包括药效学)作用效果,或确定一种或多种临床研究药品的不良反应,或监测一种或多种临床研究药品的吸收、分布、代谢和排泄,同时考虑其安全性和有效性。应当记住,临床试验可以使用药品进行。临床试验的开展必须符合临床试验参与者的权利、安全、健康和福利优先于科学和社会利益的首要原则。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
LEGAL ASPECTS OF CLINICAL TRIALS IN POLAND
A clinical trial is each trial conducted in humans to discover or confirm the clinical, pharmacological, including pharmacodynamic, effects of action of one or more investigational medicinal products, or to identify the adverse reactions to one or more investigational medicinal products, or to monitor absorption, distribution, metabolism and excretion of one or more investigational medicinal products, taking into consideration their safety and efficacy. It ought to be remembered that clinical trials may be conducted with the use of medicinal products. Clinical trials must be conducted in a way which is in line with the primary principle that clinical trial participants’ rights, safety, health, and welfare override the interest of science and society.
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