Stability Specifications
Stability Specifications is a regulatory and methodological framework within pharmaceutical development that defines the acceptable limits for physicochemical, biological, and microbiological attributes of a drug product over time, distinguishing it by establishing scientifically justified criteria to ensure safety, efficacy, and quality under specified storage conditions.
28
Publications
1.1K
Citations
91
Authors
66
Institutions
Publications per year
2017–2026
7
Variants
Stability Acceptance Criteria
Parents
28
91
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66
KU Leuven
Leuven, Belgium
1 h-index
1 publications
46 citations
Pfizer (United States)
New York, United States
1 h-index
1 publications
22 citations
United States Army
Arlington, United States
1 h-index
3 publications
69 citations
Tongji University
Shanghai, China
1 h-index
3 publications
144 citations
Haraldsplass Diakonale Sykehus
Bergen, Norway
1 h-index
1 publications
46 citations

Southeast University
Nanjing, China
1 h-index
1 publications
85 citations
AbbVie (United States)
North Chicago, United States
1 h-index
1 publications
22 citations
Regeneron (United States)
Tarrytown, United States
1 h-index
2 publications
44 citations
1–8 of 66
Repository · 4 publications · 109 citations
4
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2 publications · 218 citations
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1 publications · 46 citations
1
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1 publications · 70 citations
1
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1 publications · 24 citations
1
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