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

Authors

358

  1. MI
    Marianthi Ierapetritou

    Rutgers, The State University of New Jersey, United States

    4 publications · 361 citations

    4

    h-index

  2. MK
    Markus Krumme

    Novartis (Switzerland), Switzerland

    3 publications · 195 citations

    3

    h-index

  3. TO
    Thomas O’Connor

    Center for Drug Evaluation and Research, United States

    3 publications · 929 citations

    3

    h-index

  4. SM
    Salvatore Mascia

    USV (India), India

    3 publications · 271 citations

    3

    h-index

  5. VP
    Victoria Pauli

    Heinrich Heine University Düsseldorf, Germany

    2 publications · 78 citations

    2

    h-index

1–5 of 358

Venues

  1. Computers & Chemical Engineering

    7 publications · 476 citations

    7

    h-index

  2. Organic Process Research & Development

    7 publications · 565 citations

    7

    h-index

  3. AIChE Journal

    5 publications · 353 citations

    5

    h-index

  4. International Journal of Pharmaceutics

    4 publications · 191 citations

    4

    h-index

  5. European Journal of Pharmaceutics and Biopharmaceutics

    EJPB · 3 publications · 275 citations

    3

    h-index

1–5