Impurity Limits

Impurity Limits is a regulatory and analytical threshold, belonging to the class of quality control parameters, that specifically defines the maximum allowable level of process-related impurities in a pharmaceutical product or material as determined by safety, efficacy, and manufacturing considerations.

51

Publications

2.1K

Citations

170

Authors

98

Institutions

Publications per year

2017–2026

16

Authors

170

  1. BH
    Bjørn H. Morland

    Institute for Energy Technology, Norway

    3 publications · 192 citations

    3

    h-index

  2. DK
    David Kirkland

    Covance (United Kingdom), United Kingdom

    2 publications · 27 citations

    2

    h-index

  3. JP
    Joel P. Bercu

    Gilead Sciences (United States), United States

    2 publications · 70 citations

    2

    h-index

  4. AL
    A. Litnovsky

    Forschungszentrum Jülich, Germany

    2 publications · 44 citations

    2

    h-index

  5. GS
    Gaute Svenningsen

    Institute for Energy Technology, Norway

    2 publications · 109 citations

    2

    h-index

1–5 of 170

Venues

  1. Physical Review B

    PRB · 4 publications · 382 citations

    4

    h-index

  2. Physics of Plasmas

    3 publications · 73 citations

    3

    h-index

  3. Physical review. B./Physical review. B

    PRB · 3 publications · 60 citations

    3

    h-index

  4. Nuclear Fusion

    2 publications · 54 citations

    2

    h-index

  5. Journal of Nuclear Materials

    2 publications · 43 citations

    2

    h-index

1–5