Reference Product Availability

Reference Product Availability is a scholarly contribution representing a methodological framework within the domain of drug development and regulatory science that specifies the conditions under which an approved reference listed drug remains accessible and suitable for use in bioequivalence or comparative clinical studies.

25

Publications

946

Citations

117

Authors

57

Institutions

Publications per year

2017–2026

12

Authors

117

  1. EG
    Eileen G. Abels

    University of Maryland, College Park, United States

    1 publications · 14 citations

    1

    h-index

  2. CY
    Carolyn Y. Muller

    University of New Mexico, United States

    1 publications · 28 citations

    1

    h-index

  3. PS
    Paula Silverman

    Case Western Reserve University, United States

    1 publications · 14 citations

    1

    h-index

  4. JA
    John A. Dumot

    Cleveland Clinic, United States

    1 publications · 14 citations

    1

    h-index

  5. SH
    Shahzad Hussain

    National Institute of Health, Pakistan

    1 publications · 28 citations

    1

    h-index

1–5 of 117

Venues

  1. Future Oncology

    2 publications · 25 citations

    2

    h-index

  2. American Journal of Health-System Pharmacy

    AJHP · 1 publications · 14 citations

    1

    h-index

  3. Cutaneous and Ocular Toxicology

    1 publications · 13 citations

    1

    h-index

  4. 1

    h-index

  5. Revista Brasileira de Farmacognosia

    1 publications · 51 citations

    1

    h-index

1–5