Biosimilars: policy, clinical, and regulatory considerations.
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Biosimilars of biological drug therapies: regulatory, clinical and commercial considerations.Rituximab and biosimilars - equivalence and reciprocity.Update on the safety and bioequivalence of biosimilars - focus on enoxaparin.Biosimilars of low-molecular-weight heparin products: fostering competition or reducing 'biodiversity'?Characterization and comparison of commercially available TNF receptor 2-Fc fusion protein productsClinical concerns of immunogenicity produced at cellular levels by biopharmaceuticals following their parenteral administration into human body.Immunogenicity of botulinum toxins.Managing unexpected events in the manufacturing of biologic medicines.Efficacy and safety of biosimilar filgrastim in primary and secondary prevention of febrile neutropenia
P2860
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P2860
Biosimilars: policy, clinical, and regulatory considerations.
description
2008 nî lūn-bûn
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2008年の論文
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2008年学术文章
@wuu
2008年学术文章
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2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
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2008年學術文章
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name
Biosimilars: policy, clinical, and regulatory considerations.
@en
Biosimilars: policy, clinical, and regulatory considerations.
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type
label
Biosimilars: policy, clinical, and regulatory considerations.
@en
Biosimilars: policy, clinical, and regulatory considerations.
@nl
prefLabel
Biosimilars: policy, clinical, and regulatory considerations.
@en
Biosimilars: policy, clinical, and regulatory considerations.
@nl
P356
P1476
Biosimilars: policy, clinical, and regulatory considerations.
@en
P2093
Scott Gottlieb
P356
10.2146/AJHP080210
P433
14 Suppl 6
P577
2008-07-01T00:00:00Z