Facility Inspection

Facility Inspection is a systematic regulatory evaluation, belonging to the broader category of pharmaceutical quality assurance activities, that specifically involves the assessment of physical premises, operational practices, and documentation systems in drug manufacturing or handling sites to ensure compliance with current Good Manufacturing Practices (cGMP) and applicable regulatory standards.

97

Publications

3.1K

Citations

290

Authors

142

Institutions

Publications per year

2017–2026

16

Authors

290

  1. CW
    Chih-Hsiung Wang

    I-Shou University, Taiwan

    3 publications · 42 citations

    3

    h-index

  2. NK
    Naoto Kaio

    Hiroshima University, Japan

    2 publications · 49 citations

    2

    h-index

  3. GV
    Gopika Vinod

    Bhabha Atomic Research Centre, India

    2 publications · 60 citations

    2

    h-index

  4. SM
    Samer Madanat

    University of California, Berkeley, United States

    2 publications · 82 citations

    2

    h-index

  5. MX
    Minge Xie

    Rutgers, The State University of New Jersey, United States

    2 publications · 56 citations

    2

    h-index

1–5 of 290

Venues

  1. Management Science

    4 publications · 324 citations

    4

    h-index

  2. Reliability Engineering & System Safety

    4 publications · 142 citations

    4

    h-index

  3. 4

    h-index

  4. Journal of the Operational Research Society

    OR · 4 publications · 217 citations

    4

    h-index

  5. Computers & Industrial Engineering

    3 publications · 48 citations

    3

    h-index

1–5