Generics Equivalence Testing

Generics Equivalence Testing is a methodological framework within pharmaceutical science that establishes the bioequivalence of generic drug products to their reference listed drugs by statistically comparing dissolution profiles to ensure therapeutic equivalence.

36

Publications

1.2K

Citations

120

Authors

69

Institutions

Publications per year

2017–2026

7

Authors

120

  1. MS
    Matthias Stahl

    Technical University of Munich, Germany

    2 publications · 31 citations

    2

    h-index

  2. LG
    Luther Gwaza

    World Health Organization, Switzerland

    2 publications · 31 citations

    2

    h-index

  3. ÓV
    Ómar Vesga

    Universidad de Antioquia, Colombia

    2 publications · 62 citations

    2

    h-index

  4. OO
    Olubukola O. Oyetunde

    University of Lagos, Nigeria

    2 publications · 26 citations

    2

    h-index

  5. JW
    Jan Welink

    United States Food and Drug Administration, United States

    2 publications · 31 citations

    2

    h-index

1–5 of 120

Venues

  1. Australian Prescriber

    2 publications · 106 citations

    2

    h-index

  2. PubMed

    Repository · 2 publications · 60 citations

    2

    h-index

  3. European Journal of Clinical Pharmacology

    2 publications · 78 citations

    2

    h-index

  4. Pharmaceutical Research

    1 publications · 18 citations

    1

    h-index

  5. Journal of Pharmaceutical Sciences

    1 publications · 20 citations

    1

    h-index

1–5