Quality Evaluation and Reporting Specification for Real-World Studies of Traditional Chinese Medicine

Author:

Chai Qian-yun,Fei Yu-tong,Gao Rui,Xia Ru-yu,Lu Fang,Zi Ming-jie,Sun Ming-yue,Yang Zhong-qi,Chen Da-fang,Liu Jian-ping,

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Complementary and alternative medicine,General Medicine

Reference12 articles.

1. Wang MH, Zhao Y, Deng YZ, Xue FB, Xie HT, Yao C. Comparative study on policies, regulations and guiding principles for the application of real-world data/real-world evidence. Chin J Clin Pharmacol Therapeut (Chin) 2020;25:878–889.

2. U.S. Government. 21st Centruy Cures Act. (2016-12-13) Accessed October 1, 2021. Available at https://www.Congress.gov/114/plaws/publ255/PLAW-114publ255.pdf

3. National Medical Products Administration. Guiding principles for real-world evidence supporting drug development and review (testing version). Accessed October 1, 2021. Available at http://www.nmpa.gov.cn/WS04/CL2138/373175.html.

4. National Medical Products Administration. Special regulations on the registration and administration of traditional Chinese medicine (draft for public comment). Accessed September 6, 2021. Available at https://www.nmpa.gov.cn/xxgk/zhqyj/zhqyjyp/20200430154501315.html

5. Akobeng AK. Assessing the validity of clinical trials. J Pediatr Gastroenterol Nutr 2008;47:277–282.

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