Reference Product Availability
Reference Product Availability is a scholarly contribution representing a methodological framework within the domain of drug development and regulatory science that specifies the conditions under which an approved reference listed drug remains accessible and suitable for use in bioequivalence or comparative clinical studies.
25
Publications
946
Citations
117
Authors
57
Institutions
Publications per year
2017–2026
12
25
Approval of the first biosimilar antibodies in Europe
Alain Beck, Janice M. Reichert · mAbs · 2013 · 124 citations · Full text
1–5 of 25
117
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1
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1–5 of 117
57
Amgen (United States)
Thousand Oaks, United States
2 h-index
4 publications
79 citations
Collaborative Research Group
Sydney, Australia
1 h-index
3 publications
30 citations

University of Maiduguri
Maiduguri, Nigeria
1 h-index
1 publications
16 citations
Institute for Safe Medication Practices
Horsham, United States
1 h-index
1 publications
44 citations
Indian Institute of Technology Delhi
New Delhi, India
1 h-index
2 publications
28 citations
Michigan Medicine
Ann Arbor, United States
1 h-index
1 publications
34 citations
Procter & Gamble (Germany)
Schwalbach am Taunus, Germany
1 h-index
2 publications
26 citations
Procter & Gamble (United States)
Cincinnati, United States
1 h-index
1 publications
13 citations
1–8 of 57
2 publications · 25 citations
2
h-index
AJHP · 1 publications · 14 citations
1
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1 publications · 13 citations
1
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1 publications · 16 citations
1
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1 publications · 51 citations
1
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1–5