Interpretation of Technical Specifications for Revision of Safety Information in Marketed Chinese Patent Medicine Instructions.
10.19540/j.cnki.cjcmm.20211117.502
- Author:
Xiao-Meng ZHANG
1
;
Zhi-Jian LIN
1
;
Bing ZHANG
1
;
Ri-Na SA
1
;
Jin-Tao LYU
1
;
Hao WU
1
;
Yao-Lei LI
1
;
Hui-Zhe XU
1
;
Zheng-Kai HUANG
1
;
Yu-Bo GUO
2
;
Xiang-Fei SU
3
;
Xiao-Jiao DUAN
3
Author Information
1. School of Chinese Materia Medica,Beijing University of Chinese Medicine Beijing 102488,China Research Center for Pharmacovigilance and Rational Use of Traditional Chinese Medicine,Beijing University of Chinese Medicine Beijing 102488,China.
2. National Museum of Traditional Chinese Medicine Beijing 100027,China.
3. Standardization Office of Chinese Association of Chinese Medicine Beijing 100029,China.
- Publication Type:Journal Article
- Keywords:
Chinese patent medicine instruction;
group standard;
revision;
safety information;
technical specification
- MeSH:
China;
Drug-Related Side Effects and Adverse Reactions;
Drugs, Chinese Herbal/adverse effects*;
Humans;
Medicine, Chinese Traditional;
Nonprescription Drugs/adverse effects*;
Pharmacovigilance
- From:
China Journal of Chinese Materia Medica
2022;47(2):295-300
- CountryChina
- Language:Chinese
-
Abstract:
Technical Specifications for Revision of Safety Information in Marketed Chinese Patent Medicine Instructions,a series of group standards,were proposed by Professor ZHANG Bing from Research Center for Pharmacovigilance and Rational Use of Traditional Chinese Medicine,and underwent centralized management by Chinese Association of Chinese Medicine. They were officially released on July 23 and implemented on July 31,2021. The series of group standards consist of six sections,including general principles,adverse drug events,contraindications,precautions,application for special populations,and warnings. The section of general principles is comprised of holistic and programmatic expressions,which explain the general technical requirements for revising the marketed Chinese patent medicine instructions. The other five sections focus on information collection,screening,transformation,and illustration of specific items,forming a standardized revision technical process. This series of standards is the result of multiple rounds of research and the suggestions of more than 200 experts in different professional fields of " medicine-pharmacy-management-law-enterprise" have been gathered therein to reach a consensus. With the purposes of establishing standardized technical specifications for the revision of safety information in the marketed Chinese patent medicine instructions,guiding marketing authorization holders in revising the instructions,filling the gaps in the research of Chinese patent medicine instructions,promoting the deve-lopment of pharmaceutical care and academic research,and encouraging the rational and safe medication of Chinese patent medicine,the series of group standards is of great significance.
