Physical Stability Testing

Physical Stability Testing is a systematic analytical method used in pharmaceutical development to evaluate the resistance of a drug substance or product to changes in its physical properties under defined environmental conditions, distinguishing it from chemical stability testing by focusing exclusively on attributes such as polymorphic form, crystallinity, hygroscopicity, and solid-state morphology.

858

Publications

36.6K

Citations

3.2K

Authors

905

Institutions

Publications per year

2017–2026

345

Authors

3.2K

  1. TR
    Thomas Rades

    University of Copenhagen, Denmark

    17 publications · 1.2K citations

    15

    h-index

  2. LS
    Lynne S. Taylor

    Purdue University West Lafayette, United States

    11 publications · 914 citations

    12

    h-index

  3. LA
    Lawrence A. Trissel

    The University of Texas MD Anderson Cancer Center, United States

    14 publications · 218 citations

    11

    h-index

  4. MP
    Marian Paluch

    University of Silesia in Katowice, Poland

    10 publications · 445 citations

    10

    h-index

  5. CR
    C. Russell Middaugh

    University of Kansas, United States

    10 publications · 435 citations

    10

    h-index

1–5 of 3.2K

Venues

  1. International Journal of Pharmaceutics

    53 publications · 3.3K citations

    31

    h-index

  2. Journal of Pharmaceutical Sciences

    41 publications · 2.4K citations

    26

    h-index

  3. Food Hydrocolloids

    24 publications · 1.8K citations

    22

    h-index

  4. Molecular Pharmaceutics

    31 publications · 1.5K citations

    22

    h-index

  5. Drug Development and Industrial Pharmacy

    22 publications · 816 citations

    18

    h-index

1–5