Generic Modified-release Product Development

Generic Modified-Release Product Development is a pharmaceutical formulation strategy that involves the systematic design and optimization of bioequivalent, non-innovator modified-release dosage forms to achieve therapeutic interchangeability through controlled pharmacokinetic profiles.

6

Publications

157

Citations

42

Authors

10

Institutions

Publications per year

2017–2026

1

Authors

42

  1. TL
    Tiffany L. Correll

    Amgen (United States), United States

    1 publications · 14 citations

    1

    h-index

  2. PC
    Philipp C. Roosen

    University of California, Irvine, United States

    1 publications · 14 citations

    1

    h-index

  3. JM
    Jana Mysicka

    Mundipharma (United Kingdom), United Kingdom

    1 publications · 14 citations

    1

    h-index

  4. HR
    Harald Rettig

    Novartis (Switzerland), Switzerland

    1 publications · 14 citations

    1

    h-index

  5. AM
    A Marzo

    Sigma Tau (Italy), Italy

    1 publications · 43 citations

    1

    h-index

1–5 of 42

Venues

  1. Clinical Therapeutics

    1 publications · 26 citations

    1

    h-index

  2. PubMed

    Repository · 1 publications · 43 citations

    1

    h-index

  3. Pharmaceutical Research

    1 publications · 48 citations

    1

    h-index

  4. Clinical Drug Investigation

    1 publications · 12 citations

    1

    h-index

  5. Dissolution Technologies

    1 publications · 14 citations

    1

    h-index

1–5