Rising biosimilars in the Indian biopharmaceutical industry: emerging challenges and way forward

被引:1
|
作者
Singh, Pallavi [1 ]
Desai, Pranav N. [2 ,3 ]
Dutta, Venkatesh [1 ,4 ]
机构
[1] Babasaheb Bhimrao Ambedkar Cent Univ, DST Ctr Policy Res, Lucknow 226025, Uttar Pradesh, India
[2] Jawaharlal Nehru Univ, Ctr Res Environm Sci & Technol Policy CREST, New Delhi, India
[3] Jawaharlal Nehru Univ, Ctr Studies Sci Policy, New Delhi, India
[4] Babasaheb Bhimrao Ambedkar Cent Univ, Sch Environm Sci, Dept Environm Sci, Lucknow, Uttar Pradesh, India
关键词
Biosimilars; safety; efficacy; regulatory framework; LEARNING-PROCESSES; BIOLOGICS; EMERGENCE;
D O I
10.1080/09537325.2021.1994139
中图分类号
C93 [管理学];
学科分类号
12 ; 1201 ; 1202 ; 120202 ;
摘要
Biopharmaceuticals have the potential to contribute immensely towards improving the health and quality of life of people. However, there is a gap in the availability of medical services in India and inequality in disseminating health benefits to the poor. Several issues are associated with biopharmaceuticals, such as increasing cost of treatments, access, affordability, safety, efficacy, quality, and intellectual property rights. Hence, the present paper addresses the crucial questions on the emerging challenges in the Indian biopharmaceutical industry regarding the patent cliff and biosimilars. What are the technological and institutional challenges faced by the biosimilars producing firms? Whether biosimilars could meet the regulatory requirements of safety, efficacy, and whether they will meet global regulatory standards? This article further analyses the regulatory pathways for commercial approval of biosimilars.
引用
收藏
页码:1145 / 1160
页数:16
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