Impurity Reference Standard Development

Impurity Reference Standard Development is the systematic process of creating and validating authentic chemical specimens of impurities for use as benchmarks in the identification, characterization, and quantification of unintended components within pharmaceutical substances and products.

22

Publications

818

Citations

121

Authors

53

Institutions

Publications per year

2017–2026

5

Authors

121

  1. MG
    M. Gil

    Universidad Politécnica de Madrid, Spain

    1 publications · 54 citations

    1

    h-index

  2. SK
    Sanjay Kumar

    National Institute of Pharmaceutical Education and Research, India

    1 publications · 26 citations

    1

    h-index

  3. SS
    Syed Salman Lateef

    University of Illinois Chicago, United States

    1 publications · 28 citations

    1

    h-index

  4. FA
    Frankie Aiello

    German Jordanian University, Jordan

    1 publications · 28 citations

    1

    h-index

  5. VS
    Valnei S. Cunha

    Instituto Nacional de Metrologia, Qualidade e Tecnologia, Brazil

    1 publications · 11 citations

    1

    h-index

1–5 of 121

Venues

  1. 7

    h-index

  2. TrAC Trends in Analytical Chemistry

    2 publications · 144 citations

    2

    h-index

  3. BUNSEKI KAGAKU

    1 publications · 18 citations

    1

    h-index

  4. Analytical Methods

    1 publications · 23 citations

    1

    h-index

  5. Chromatographia

    1 publications · 21 citations

    1

    h-index

1–5