Aseptic Process Validation

Aseptic Process Validation is a formal qualification process within pharmaceutical manufacturing that demonstrates the consistent ability of an aseptic system to prevent microbiological contamination during the sterilization, handling, and assembly of sterile drug products, thereby ensuring product sterility and patient safety.

12

Publications

219

Citations

52

Authors

17

Institutions

Publications per year

2017–2026

2

Authors

52

  1. KE
    K. E. Stevenson

    Michigan State University, United States

    2 publications · 25 citations

    2

    h-index

  2. SC
    Sue Crow

    Louisiana State University, United States

    1 publications · 12 citations

    1

    h-index

  3. DT
    Dane T. Bernard

    National Governors Association, United States

    1 publications · 12 citations

    1

    h-index

  4. VN
    Virginia N. Scott

    National Governors Association, United States

    1 publications · 12 citations

    1

    h-index

  5. ME
    Martin Ehmann

    University Hospital Heidelberg, Germany

    1 publications · 15 citations

    1

    h-index

1–5 of 52

Venues

  1. American Journal of Health-System Pharmacy

    AJHP · 2 publications · 34 citations

    2

    h-index

  2. The Lancet

    2 publications · 55 citations

    2

    h-index

  3. Food Control

    1 publications · 23 citations

    1

    h-index

  4. Sensors and Actuators A Physical

    1 publications · 14 citations

    1

    h-index

  5. Journal of Oncology Pharmacy Practice

    1 publications · 18 citations

    1

    h-index

1–5