Impurity Profiling Method Development
Impurity Profiling Method Development is a methodological contribution in analytical chemistry that involves the systematic design and optimization of analytical procedures specifically intended to identify, characterize, and quantify impurities in pharmaceutical substances or products, distinguishing it from other method development processes by its exclusive focus on impurity detection, structural elucidation, and stability-indicating capability.
120
Publications
3.8K
Citations
505
Authors
157
Institutions
Publications per year
2017–2026
19
Parents
120
1–5 of 120
505
11
h-index
5
h-index
4
h-index
4
h-index
4
h-index
1–5 of 505
157
Gedeon Richter (Hungary)
Budapest, Hungary
13 h-index
59 publications
2.2K citations
Eli Lilly (United States)
Indianapolis, United States
5 h-index
15 publications
445 citations
Vrije Universiteit Brussel
Brussels, Belgium
4 h-index
13 publications
606 citations
Dr. Reddy's Laboratories (India)
Hyderabad, India
4 h-index
24 publications
570 citations
Jawaharlal Nehru Technological University, Hyderabad
Hyderabad, India
4 h-index
5 publications
117 citations
Pfizer (United States)
New York, United States
3 h-index
20 publications
916 citations
AstraZeneca (Sweden)
Södertälje, Sweden
3 h-index
7 publications
282 citations

Cairo University
Giza, Egypt
3 h-index
10 publications
225 citations
1–8 of 157
44 publications · 1.1K citations
23
h-index
8 publications · 256 citations
8
h-index
5 publications · 104 citations
5
h-index
4 publications · 206 citations
4
h-index
4 publications · 411 citations
4
h-index
1–5