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1.
China Journal of Chinese Materia Medica ; (24): 1711-1716, 2021.
Article Dans Chinois | WPRIM | ID: wpr-879084

Résumé

Since the safety re-evaluation of traditional Chinese medicine(TCM) injections began in 2009, some TCM injection companies and research institutes have done a lot of work. And with the increase of drug development and drug production technology levels in China, the safety of some TCM injections has been greatly improved. There are safety risks in TCM injections, which are mainly reflected in unclear basis of medicinal materials, simple production process, poor controllability of quality standards, nonstan-dard drug instructions and irrational medication in the use process. This paper describes the research progress of the above-mentioned aspects of TCM injections. In addition, the author team found that adverse reactions of TCM injections are mainly pseudo-allergic reactions. Therefore, a lot of work has been done in detection of pseudo-allergic reactions, mechanism research and risk control. This part of the work is also described in this article.


Sujets)
Humains , Chine , Médicaments issus de plantes chinoises/effets indésirables , Hypersensibilité/étiologie , Injections , Médecine traditionnelle chinoise/effets indésirables
2.
World Science and Technology-Modernization of Traditional Chinese Medicine ; (12): 1433-1436, 2013.
Article Dans Chinois | WPRIM | ID: wpr-441629

Résumé

It has been widely accepted in modern pharmaceutical industry that quality cannot be tested into products , instead quality should be built-in by design . However , the implementation of Quality by Design ( QbD ) in development , manufacture and supervision of traditional Chinese medicine ( TCM ) still remains to be a challenge . The program of safety re-evaluation of TCM injections provides an opportunity to practice QbD approach in TCM industry . This paper discussed some potential ways that improve the quality of TCM injec-tions base on QbD related tools , including identification of critical quality attributes , critical process parameters and critical material attributes, development of design space and control strategy.

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