Biosimilars: A consideration of the regulations in the United States and European union-Reference-Cited by-同舟云学术

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Biosimilars: A consideration of the regulations in the United States and European union

Published:2016-04 Issue: Volume:76 Page:199-208
ISSN:0273-2300
Container-title:Regulatory Toxicology and Pharmacology
language:en
Short-container-title:Regulatory Toxicology and Pharmacology

Author:

Daller Justin

Publisher

Elsevier BV

Subject

Toxicology,General Medicine

Reference45 articles.

1. Considerations in the early development of biosimilar products;Li;Drug Discov. Today,2015

3. ASBM Biosimilars Survey;Alliance for Safe Biologic Medicine,2012

4. Biologics and Biosimilars: an Overview;AMGEN.,2014

5. Biosimilars in 2014: an Interview with FDA New Drugs Head John Jenkins;Bagdhdadi,2014

Cited by 60 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

2. Infliximab biosimilar GP1111: a review of 5 years’ post-approval experience;Expert Opinion on Biological Therapy;2024-07-02

3. Obstacles to Biosimilar Acceptance and Uptake in Oncology;JAMA Oncology;2024-07-01

4. Clinical and Economic Value of a Biosimilar Portfolio to Stakeholders: An Integrative Literature Review;ClinicoEconomics and Outcomes Research;2024-05

5. Cancer treatment with biosimilar drugs: A review;Cancer Innovation;2024-04

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