Continued Process Verification

Continued Process Verification is a stage of pharmaceutical process validation that consists of the ongoing, statistically based collection and evaluation of manufacturing and quality data during routine production to demonstrate and maintain a state of control and the consistent achievement of predetermined product quality attributes.

9

Publications

304

Citations

49

Authors

21

Institutions

Publications per year

2017–2026

5

Authors

49

  1. EM
    Ehab M. Moussa

    Assiut University, Egypt

    2 publications · 52 citations

    2

    h-index

  2. AA
    Alina Alexeenko

    Purdue University West Lafayette, United States

    2 publications · 52 citations

    2

    h-index

  3. PS
    Puneet Sharma

    Thapar Institute of Engineering & Technology, India

    2 publications · 52 citations

    2

    h-index

  4. PK
    Petr Kazarin

    Purdue University West Lafayette, United States

    2 publications · 52 citations

    2

    h-index

  5. JA
    Joseph Azzarella

    Fresenius Kabi (United States), United States

    2 publications · 52 citations

    2

    h-index

1–5 of 49

Venues

  1. AAPS PharmSciTech

    2 publications · 52 citations

    2

    h-index

  2. Biotechnology Progress

    1 publications · 10 citations

    1

    h-index

  3. Data in Brief

    1 publications · 13 citations

    1

    h-index

  4. The AAPS Journal

    AAPSJ · 1 publications · 112 citations

    1

    h-index

  5. Biotechnology and Bioengineering

    1 publications · 54 citations

    1

    h-index

1–5