Stability Specifications

Stability Specifications is a regulatory and methodological framework within pharmaceutical development that defines the acceptable limits for physicochemical, biological, and microbiological attributes of a drug product over time, distinguishing it by establishing scientifically justified criteria to ensure safety, efficacy, and quality under specified storage conditions.

28

Publications

1.1K

Citations

91

Authors

66

Institutions

Publications per year

2017–2026

7

Variants

Stability Acceptance Criteria

Authors

91

  1. RC
    Rong Chen

    Dalian Maritime University, China

    1 publications · 45 citations

    1

    h-index

  2. GJ
    G. J. Iafrate

    United States Department of the Army, United States

    1 publications · 23 citations

    1

    h-index

  3. GB
    Gunn B.B. Kristensen

    Odense University Hospital, Denmark

    1 publications · 46 citations

    1

    h-index

  4. AC
    Adithi C. Bhargava

    AbbVie (United States), United States

    1 publications · 22 citations

    1

    h-index

  5. ES
    Esther Sanabria Codesal

    Universitat Politècnica de València, Spain

    1 publications · 11 citations

    1

    h-index

1–5 of 91

Venues

  1. PubMed

    Repository · 4 publications · 109 citations

    4

    h-index

  2. Drug Development and Industrial Pharmacy

    2 publications · 218 citations

    2

    h-index

  3. 1

    h-index

  4. Asian Journal of Control

    1 publications · 70 citations

    1

    h-index

  5. International Journal of Cosmetic Science

    1 publications · 24 citations

    1

    h-index

1–5