Calibration - The USP dissolution apparatus suitability test

Drug Information Journal

Volumn 30, Issue 4, 1996, Pages 1055-1061

  Qureshi, Saeed A ^a  

^a Bureau of Drug Research   (Canada)

Author keywords

Apparatus; Drug dissolution; United States Pharmacopeia

Indexed keywords

FUROSEMIDE; PREDNISONE; SALICYLIC ACID DERIVATIVE;

APPARATUS; CALIBRATION; DRUG MANUFACTURE; DRUG QUALITY; DRUG RELEASE; DRUG SOLUBILITY; MEDICAL LITERATURE; PHARMACEUTICS; PRACTICE GUIDELINE; PRIORITY JOURNAL; REVIEW; TABLET; TABLET DISINTEGRATION; UNITED STATES;

EID: 0029807072     PISSN: 00928615     EISSN: None     Source Type: Journal    
DOI: 10.1177/009286159603000422     Document Type: Review

References (9)

1. United States Pharmacopeia (USP) XXIII, Rockville, MD, 1995:1791-1793.
2. The USP Dissolution Calibrator Tablet Collaborative Study - An Overview of the Fourth Quarter 1994 Process. Pharmacop For. 1995;21:841-858.
3. Grady LT. Dissolution Calibrators Used by the United States Pharmacopeia. Pharmacop For. 1994;20:8567-8570.
4. Gray VA, Hubert BB. Calibration of Dissolution Apparatuses. 1 and 2 - What to Do When Equipment Fails. Pharmacop For. 1994;20:8571-73.
5. Achanta AS, Gray VA, Cecil TL, Grady LT. Evaluation of the Performance of Prednisone and Salicylic Acid Calibrators. Drug Dev Ind Pharm. 1995;21(10): 1171-1182.
6. Drugs Directorate Guidelines "Acceptable Methods," Ottawa, Canada: Canadian Government Publishing Centre, Supply and Services Canada; 1994.
7. Qureshi SA, McGilveray IJ. Impact of Different Deaeration Methods on the USP Dissolution Apparatus Suitability Test Criteria. Pharmacop For. 1994;20: 8565-8566.
8. Qureshi SA, McGilveray IJ. A Critical Assessment of the USP Dissolution Apparatus Suitability Test Criteria. Drug Dev Ind Pharm. 1995;21(8):905-924.
9. McCormick TJ. Industry Perspective on Dissolution Apparatus Calibration. Dissolution Tech. 1995;2: 12-15.