Experiences with USP apparatus 4 calibration

Dissolution Technologies

Volumn 12, Issue 2, 2005, Pages 33-39

  Krämer, Johannes ^a   Stippler, Erika ^a  

^a PHAST GmbH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

PREDNISONE; SALICYLIC ACID;

ANALYTIC METHOD; ANALYTICAL EQUIPMENT; CALIBRATION; CONTROLLED STUDY; DISSOLUTION RATE CONSTANT; DISSOLUTION TESTING; DRUG DELIVERY SYSTEM; DRUG DOSAGE FORM; DRUG FORMULATION; DRUG RELEASE; DRUG SOLUBILITY; FLOW RATE; FLOW THROUGH CELL APPARATUS; GOOD MANUFACTURING PRACTICE; IN VITRO STUDY; INSTRUMENT VALIDATION; NOTE; SUPPOSITORY; TABLET; TABLET DISINTEGRATION; USP APPARATUS 4;

EID: 84962068356     PISSN: 1521298X     EISSN: None     Source Type: Journal    
DOI: 10.14227/DT120205P33     Document Type: Note

References (3)

1. Gray, V. A., Drug Release Calibrators for Apparatus 3-Collaborative Study Results, Pharm. Forum 20, I (1994), 6934-6943
2. Dressman, Krämer, eds. Dissolution Testing of Oral Dosage Forms, published by Marcel Dekker, New York, 2005.
3. Hanson, R and Gray V, Handbook of Dissolution Testing, Third Edition, 2004, published by Dissolution Technologies, Inc., Hockessin, DE.