Parenteral Formulation Stability

Parenteral Formulation Stability is the scientific assessment of the maintenance of physicochemical and microbiological integrity of a parenteral formulation under specified storage conditions over time, distinguishing it from other pharmaceutical stability evaluations by its exclusive focus on sterile, non-oral dosage forms intended for administration via routes such as intravenous, intramuscular, or subcutaneous injection.

65

Publications

1.7K

Citations

277

Authors

113

Institutions

Publications per year

2017–2026

7

Authors

277

  1. BN
    Bastiaan Nuijen

    The Netherlands Cancer Institute, Netherlands

    3 publications · 63 citations

    2

    h-index

  2. DW
    Dorota Wątróbska-Świetlikowska

    Gdańsk Medical University, Poland

    2 publications · 27 citations

    2

    h-index

  3. GT
    George Tsallas

    Toronto General Hospital, Canada

    2 publications · 29 citations

    2

    h-index

  4. SE
    Scott E. Walker

    Sunnybrook Health Science Centre, Canada

    2 publications · 45 citations

    2

    h-index

  5. RD
    Ralph D. Feigin

    St. Louis Children's Hospital, United States

    2 publications · 36 citations

    2

    h-index

1–5 of 277

Venues

  1. American Journal of Health-System Pharmacy

    AJHP · 8 publications · 160 citations

    9

    h-index

  2. PubMed

    Repository · 9 publications · 194 citations

    9

    h-index

  3. Journal of Parenteral and Enteral Nutrition

    5 publications · 122 citations

    5

    h-index

  4. Drug Development and Industrial Pharmacy

    4 publications · 87 citations

    4

    h-index

  5. International Journal of Pharmaceutics

    4 publications · 126 citations

    4

    h-index

1–5