Solid Dosage Form Analysis
Solid Dosage Form Analysis is a pharmaceutical analytical method that involves the systematic examination and characterization of solid medicinal formulations, distinguished by its focus on evaluating the physical, chemical, and functional properties of drugs in solid forms such as tablets, capsules, and powders to ensure identity, purity, potency, and quality.
158
Publications
5.4K
Citations
567
Authors
196
Institutions
Publications per year
2017–2026
30
Parents
158
Jacques Bourquin, Heinz Schmidli, Peter van Hoogevest et al. · European Journal of Pharmaceutical Sciences · 1998 · 141 citations
1–5 of 158
567
3
h-index
3
h-index
3
h-index
3
h-index
2
h-index
1–5 of 567
196
Pfizer (United States)
New York, United States
5 h-index
7 publications
438 citations

Centre National de la Recherche Scientifique
Paris, France
4 h-index
13 publications
869 citations
Merck & Co., Inc., Rahway, NJ, USA (United States)
Rahway, United States
4 h-index
12 publications
491 citations

University of Minnesota
Minneapolis, United States
3 h-index
5 publications
143 citations
Purdue University West Lafayette
West Lafayette, United States
3 h-index
6 publications
668 citations

Dr. Reddy's Laboratories (United States)
Princeton, United States
3 h-index
6 publications
137 citations

University of Otago
Dunedin, New Zealand
3 h-index
11 publications
1.1K citations

Cairo University
Giza, Egypt
3 h-index
6 publications
117 citations
1–8 of 196
15 publications · 673 citations
13
h-index
9 publications · 361 citations
9
h-index
8 publications · 377 citations
8
h-index
7 publications · 168 citations
7
h-index
7 publications · 179 citations
7
h-index
1–5