Quality Control in Compounding is a systematic process within pharmaceutical practice that verifies the accuracy, sterility, and consistency of compounded preparations through standardized testing and procedural validation to ensure compliance with established pharmacopeial and regulatory standards.
5
Publications
83
Citations
16
Authors
11
Institutions
Publications per year
2017–2026
2
Parents
Publications
5
Validation of an automated method for compounding monoclonal antibody patient doses
Bas Peters, Martinus A.H. Capelle, Tudor Arvinte et al. · mAbs · 2013 · 23 citations · Full text
Pharmacy, Immunology, Pharmaceutics +17
1–5 of 5
Authors
16
- CD
1
h-index
- CR
1
h-index
- LH
1
h-index
- SA
1
h-index
- KEKenneth E. Avis
University of Tennessee Health Science Center, United States
1 publications · 14 citations
1
h-index
1–5 of 16
Institutions
11
University of Lagos
Lagos, Nigeria
1 h-index
1 publications
14 citations
Houston Methodist
Houston, United States
1 h-index
1 publications
14 citations
University of Geneva
Geneva, Switzerland
1 h-index
1 publications
23 citations
Nieuwegein Fonds
Nieuwegein, Netherlands
1 h-index
2 publications
46 citations
Methodist University Hospital
Memphis, United States
1 h-index
1 publications
14 citations
St. John Fisher College
Rochester, United States
1 h-index
2 publications
34 citations
University of Lausanne
Lausanne, Switzerland
1 h-index
1 publications
23 citations
National and Kapodistrian University of Athens
Athens, Greece
1 h-index
3 publications
33 citations
1–8 of 11
Venues
- mAbs
1 publications · 23 citations
1
h-index
- American Journal of Health-System Pharmacy
AJHP · 1 publications · 14 citations
1
h-index
- Global Drugs and Therapeutics
GDT · 1 publications · 11 citations
1
h-index
- New England Journal of Medicine
NEJM · 1 publications · 18 citations
1
h-index
- American Journal of Pharmaceutical Education
1 publications · 17 citations
1
h-index
1–5