Interchangeability Rules
Interchangeability Rules is a regulatory framework within step therapy policies that specifies the criteria and conditions under which one pharmaceutical agent may be substituted for another in a treatment sequence, based on demonstrated therapeutic equivalence and safety.
15
Publications
561
Citations
45
Authors
34
Institutions
Publications per year
2017–2026
5
Parents
15
Patent Scope and Innovation in the Software Industry
Julie E. Cohen · California Law Review · 2001 · 105 citations · Full text
A ‘Global Reference’ Comparator for Biosimilar Development
Chris Webster, Gillian R. Woollett · BioDrugs · 2017 · 43 citations · Full text
1–5 of 15
45
3
h-index
3
h-index
2
h-index
2
h-index
United States Food and Drug Administration, United States
2 publications · 43 citations
2
h-index
1–5 of 45
34
Apotex (Canada)
Toronto, Canada
2 h-index
2 publications
43 citations
United States Food and Drug Administration
Silver Spring, United States
2 h-index
6 publications
129 citations
Georgetown University
Washington, United States
2 h-index
2 publications
185 citations
Teva Pharmaceuticals (United States)
North Wales, United States
2 h-index
2 publications
43 citations
International Pharmaceutical Federation
The Hague, Netherlands
2 h-index
2 publications
43 citations
SocraTec R&D (Germany)
Erfurt, Germany
2 h-index
2 publications
43 citations
Merck & Co., Inc., Rahway, NJ, USA (United States)
Rahway, United States
2 h-index
2 publications
43 citations
University of Lisbon
Lisbon, Portugal
2 h-index
2 publications
43 citations
1–8 of 34
2 publications · 247 citations
2
h-index
JECCM · 1 publications · 34 citations
1
h-index
1 publications · 27 citations
1
h-index
CMRO · 1 publications · 12 citations
1
h-index
1 publications · 14 citations
1
h-index
1–5