Impurity Limits
Impurity Limits is a regulatory and analytical threshold, belonging to the class of quality control parameters, that specifically defines the maximum allowable level of process-related impurities in a pharmaceutical product or material as determined by safety, efficacy, and manufacturing considerations.
51
Publications
2.1K
Citations
170
Authors
98
Institutions
Publications per year
2017–2026
16
Parents
51
New method for the Anderson model
S. E. Barnes · Journal of Physics F Metal Physics · 1976 · 498 citations
Elastic scattering theory and transport in graphene
Dmitry S. Novikov · Physical Review B · 2007 · 257 citations · Full text
Friedel oscillations and the Kondo screening cloud
Ian Affleck, L. Borda, Hubert Saleur · Physical Review B · 2008 · 85 citations · Full text
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98

Institute for Energy Technology
Lillestrøm, Norway
3 h-index
9 publications
576 citations
Princeton University
Princeton, United States
3 h-index
5 publications
388 citations
Bristol-Myers Squibb (United States)
New York, United States
2 h-index
3 publications
86 citations
Max Planck Institute for Plasma Physics
Garching, Germany
2 h-index
4 publications
140 citations
Forschungszentrum Jülich
Jülich, Germany
2 h-index
17 publications
424 citations
Pfizer (United States)
New York, United States
2 h-index
5 publications
190 citations
PAREXEL International (United Kingdom)
Birmingham, United Kingdom
2 h-index
2 publications
27 citations
Takeda (United States)
Deerfield, United States
2 h-index
2 publications
64 citations
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PRB · 4 publications · 382 citations
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3 publications · 73 citations
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PRB · 3 publications · 60 citations
3
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2 publications · 54 citations
2
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2 publications · 43 citations
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