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中国儿科药物评价的监管考虑因素。

Regulatory considerations for paediatric drug evaluation in China.

机构信息

Centre for Drug Evaluation, National Medical Products Administration, Beijing, People's Republic of China.

Department of Clinical Pharmacy, Key Laboratory of Chemical Biology (Ministry of Education), School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, People's Republic of China.

出版信息

BMJ Paediatr Open. 2023 May;7(1). doi: 10.1136/bmjpo-2022-001666.

Abstract

The regulatory guidelines for the research and development of paediatric drugs are still evolving in China. The formulation of the guidelines started from learning and borrowing existing experience, and gradually changed to the exploration and improvement of local guidelines, which was not only in line with international standards but also had breakthroughs, innovations and Chinese characteristics. In this paper, the current setting of paediatric drug research and development in China and corresponding technical guidelines have been introduced from regulatory perspectives, and the accessibility of further improvement in regulatory strategies has also been discussed.

摘要

在中国,儿童药物研发的监管指导原则仍在不断发展。指导原则的制定从学习和借鉴现有经验开始,逐步转变为探索和完善本土指导原则,这不仅符合国际标准,还有所突破、创新并具有中国特色。本文从监管角度介绍了中国目前儿童药物研发的现状和相应的技术指导原则,并探讨了监管策略进一步完善的可及性。

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