Solid Dosage Form Analysis

Solid Dosage Form Analysis is a pharmaceutical analytical method that involves the systematic examination and characterization of solid medicinal formulations, distinguished by its focus on evaluating the physical, chemical, and functional properties of drugs in solid forms such as tablets, capsules, and powders to ensure identity, purity, potency, and quality.

158

Publications

5.4K

Citations

567

Authors

196

Institutions

Publications per year

2017–2026

30

Publications

158

Authors

567

  1. BC
    Bruno C. Hancock

    Pfizer (United States), United States

    3 publications · 198 citations

    3

    h-index

  2. JR
    Jukka Rantanen

    University of Copenhagen, Denmark

    3 publications · 191 citations

    3

    h-index

  3. YR
    Yves Roggo

    Roche (Switzerland), Switzerland

    3 publications · 200 citations

    3

    h-index

  4. MW
    Marek Wesołowski

    Gdańsk Medical University, Poland

    3 publications · 72 citations

    3

    h-index

  5. ÇÇ
    Çetin Çetinkaya

    Clarkson University, United States

    2 publications · 63 citations

    2

    h-index

1–5 of 567

Venues

  1. 13

    h-index

  2. Journal of Pharmaceutical Sciences

    9 publications · 361 citations

    9

    h-index

  3. International Journal of Pharmaceutics

    8 publications · 377 citations

    8

    h-index

  4. Drug Development and Industrial Pharmacy

    7 publications · 168 citations

    7

    h-index

  5. Indian Journal of Pharmaceutical Sciences

    7 publications · 179 citations

    7

    h-index

1–5