Pharmaceutical Batch Processing
Pharmaceutical Batch Processing is a systematic manufacturing approach within batch process systems in which a finite quantity of a pharmaceutical product is produced through a sequence of defined, validated, and documented steps that ensure quality, traceability, and compliance with regulatory standards, distinguishing it from continuous or general industrial batch processing by its adherence to stringent Good Manufacturing Practices (GMP) and patient-safety-critical quality controls.
79
Publications
4.1K
Citations
358
Authors
131
Institutions
Publications per year
2017–2026
27
Parents
79
Peter Poechlauer, Julie B. Manley, Rinus Broxterman et al. · Organic Process Research & Development · 2012 · 176 citations
Engineering, Chemical Engineering, Manufacturing Engineering +17
1–5 of 79
358
Rutgers, The State University of New Jersey, United States
4 publications · 361 citations
4
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3
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3
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3
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2
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1–5 of 358
131
Rutgers, The State University of New Jersey
New Brunswick, United States
6 h-index
20 publications
1K citations
Eli Lilly (United States)
Indianapolis, United States
4 h-index
22 publications
1.4K citations
Novartis (Switzerland)
Basel, Switzerland
4 h-index
11 publications
523 citations
Pfizer (United States)
New York, United States
4 h-index
12 publications
458 citations
Center for Drug Evaluation and Research
Silver Spring, United States
3 h-index
26 publications
8.4K citations
Heinrich Heine University Düsseldorf
Düsseldorf, Germany
3 h-index
6 publications
442 citations

Ghent University
Ghent, Belgium
3 h-index
8 publications
286 citations
University of Lisbon
Lisbon, Portugal
2 h-index
3 publications
76 citations
1–8 of 131
7 publications · 476 citations
7
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7 publications · 565 citations
7
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5 publications · 353 citations
5
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4 publications · 191 citations
4
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EJPB · 3 publications · 275 citations
3
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1–5