Compounded products - Stability studies in Hospital Pharmacy Departments

Journal of Pharmacy Practice and Research

Volumn 39, Issue 1, 2009, Pages 5-7

  Prankerd, Richard J ^a  

^a MONASH UNIVERSITY   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

DRUG; OXYTOCIN;

ACCURACY; DRUG DEGRADATION; DRUG DETERMINATION; DRUG FORMULATION; DRUG INCOMPATIBILITY; DRUG ISOLATION; DRUG QUALITY; DRUG STABILITY; DRUG STORAGE; EDITORIAL; ELUTION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HOSPITAL PHARMACY; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE; PHARMACIST ATTITUDE; SENSITIVITY ANALYSIS; VALIDATION PROCESS;

EID: 65549109003     PISSN: 1445937X     EISSN: None     Source Type: Journal    
DOI: 10.1002/j.2055-2335.2009.tb00693.x     Document Type: Editorial

References (8)

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3. Prankerd RJ. Practical aspects of stability testing. Aust J Hosp Pharm 1995; 25: 405-8.
4. Riley CM. Statistical parameters and analytical figures of merit. In: Riley CM, Rosanske TW, authors. Development and validation of analytical methods. Oxford: Pergamon Press; 1996.
5. Dolan JW. Stability-indicating assays. LC-GC North America 2004; 25: 346-8.
6. Center for Drug Evaluation and Research. Reviewer guidance: validation of chromatographic methods. Washington: Center for Drug Evaluation and Research; 1994. Available from .
7. Bianchini RM, Castellano PM, Kaufman TS. Validated stability-indicating HPLC method for the determination of pridinol mesylate. J Pharm Biomed Anal 2008; 48: 1151-60.
8. Sharley NA, Yu AM, Williams DB. Stability of mixtures formulated from warfarin tablets or powder. J Pharm Pract Res 2007; 37: 95-7.