Aseptic Process Qualification

Aseptic Process Qualification is a formal validation methodology within pharmaceutical microbiology that establishes the capability of an aseptic manufacturing process to consistently produce sterile dosage forms by demonstrating the absence of microbial contamination under defined operating conditions.

2

Publications

27

Citations

12

Authors

3

Institutions

Publications per year

2017–2026

0

Authors

12

  1. MM
    Mieke Mertens

    University Hospital Heidelberg, Germany

    1 publications · 15 citations

    1

    h-index

  2. ED
    Elaine Daniell

    Medical Protective, United States

    1 publications · 12 citations

    1

    h-index

  3. TS
    T Schoening

    University Hospital Heidelberg, Germany

    1 publications · 15 citations

    1

    h-index

  4. AS
    A Sancho Artés

    University Hospital Heidelberg, Germany

    1 publications · 15 citations

    1

    h-index

  5. MA
    Manuel Almeida Saavedra

    University of Arizona, United States

    1 publications · 12 citations

    1

    h-index

1–5 of 12

Institutions

3

  1. Medical Protective

    Fort Wayne, United States

    1 h-index

    1 publications

    12 citations

  2. University Hospital Heidelberg

    Heidelberg, Germany

    1 h-index

    6 publications

    90 citations

  3. Heidelberg University

    Heidelberg, Germany

    1 h-index

    6 publications

    90 citations

1–3 of 3

Venues

  1. European Journal of Hospital Pharmacy

    EJHP · 1 publications · 15 citations

    1

    h-index

  2. Biomedical Instrumentation & Technology

    BI&T · 1 publications · 12 citations

    1

    h-index

1–2