A Systematic Review of U.S. Biosimilar Approvals: What Evidence Does the FDA Require and How Are Manufacturers Responding?-Reference-Cited by-同舟云学术

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A Systematic Review of U.S. Biosimilar Approvals: What Evidence Does the FDA Require and How Are Manufacturers Responding?

Published:2017-12 Issue:12 Volume:23 Page:1234-1244
ISSN:2376-0540
Container-title:Journal of Managed Care & Specialty Pharmacy
language:en
Short-container-title:JMCP

Author:

Hung Anna¹,Vu Quyen¹,Mostovoy Lisa²

Affiliation:

1. University of Maryland School of Pharmacy, Baltimore, and Federal Employee Program, BlueCross BlueShield Association, Washington, DC.

2. Federal Employee Program, BlueCross BlueShield Association, Washington, DC.

Publisher

Academy of Managed Care Pharmacy

Subject

Health Policy,Pharmaceutical Science,Pharmacy

Cited by 24 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

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

2. INVESTIGATING THE PHYSICOCHEMICAL, NON-CLINICAL, AND CLINICAL CRITERIA FOR ASSESSING COMPARABILITY IN RANIBIZUMAB BIOSIMILARS: A COMPREHENSIVE REVIEW;FARMACIA;2024

3. A comprehensive review and analysis of patents on biological and biosimilar products listed in the purple book;World Patent Information;2024-03

4. Regulatory Considerations of Biosimilars in Cancer;Biosimilars for Cancer Treatment;2024

5. Biosimilars in Blood Cancer;Biosimilars for Cancer Treatment;2024

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