Highlights of the AAPS workshop on dissolution testing for the 21st century

Dissolution Technologies

Volumn 13, Issue 3, 2006, Pages 26-31

  Parker, Jan ^a   Gray, Vivian ^b  

^a Lancaster Laboratories   (United States)

^b V A GRAY CONSULTING INC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENERIC DRUG;

ANALYTIC METHOD; BIOEQUIVALENCE; DISSOLUTION; DISSOLUTION TESTING; DRUG BIOAVAILABILITY; DRUG DESIGN; DRUG DOSAGE FORM; DRUG EFFICACY; DRUG ELUTING STENT; DRUG RELEASE; DRUG RESEARCH; DRUG SAFETY; DRUG SOLUBILITY; DRUG STABILITY; HYDRODYNAMICS; IN VITRO STUDY; INSTRUMENT VALIDATION; NOTE; PARTICLE SIZE; PARTICLE SIZE ANALYSIS; PARTICLE SIZE DISTRIBUTION; PHARMACIST; QUALITY CONTROL; UNITED STATES; WORKSHOP;

EID: 84962087226     PISSN: 1521298X     EISSN: None     Source Type: Journal    
DOI: 10.14227/DT130306P26     Document Type: Note

References (0)