Creating China's Biosimilar Drugs Regulatory System: A Calculated Approach
Front Pharmacol
.
2022 Feb 2:13:815074.
doi: 10.3389/fphar.2022.815074.
eCollection 2022.
Authors
Jianhong Yang
1
,
Xiaoyu Zhao
1
,
Jie Li
2
,
Kejian Zhang
1
3
4
,
Zheru Zhang
5
,
Shunwen Chang
6
,
Daotian Fu
7
,
Xinhuan Lyu
1
,
Xianglin Zhang
1
,
Ying Shao
1
Affiliations
1
Research center of Yeehong Business School, Shenyang Pharmaceutical University, Beijing, China.
2
Overland Pharma (Shanghai) Limited Company, Shanghai, China.
3
School of Pharmaceuticals, Sun Yat-sen University, Guangzhou, China.
4
South China Center for Innovative Pharmaceuticals, Guangdong, China.
5
I-Mab, Shanghai, China.
6
Skyline Therapeutics, Shanghai, China.
7
RemeGen, Ltd., Shandong, China.
PMID:
35185570
PMCID:
PMC8848751
DOI:
10.3389/fphar.2022.815074
No abstract available
Keywords:
biosimilar drug; efficacy; law and regulation; safety; supervision.