CRS/AAPS joint workshop on critical variables in the in vitro and in vivo performance of Parenteral Sustained-Release Products

Dissolution Technologies

Volumn 16, Issue 2, 2009, Pages 55-56

  Rathbone, Michael J ^a   Martinez, Marilyn N ^b   Huynh, Mai ^b   Burgess, Diane ^c  

^a GRIFFITH UNIVERSITY   (Australia)

^b CENTER FOR DRUG EVALUATION AND RESEARCH   (United States)

^c UNIVERSITY OF CONNECTICUT   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 69349085231     PISSN: 1521298X     EISSN: None     Source Type: Journal    
DOI: 10.14227/DT160209P55     Document Type: Article

References (2)

1. Martinez, M.; Rathbone, M.; Burgess, D.; Huynh, M. In vitro and in vivo considerations associated with parenteral sustained release products: A review based upon information presented and points expressed at the 2007 Controlled Release Society Annual Meeting. J. Controlled Release 2008, 129 (2), 79-87.
2. Martinez, M.; Huynh, M.; Burgess, D.; Rathbone, M. Defining the Critical Quality Attributes of Modified Release Parenteral Dosage Forms: Opportunities for Ongoing Dialogue. CRS Newsletter 2008, 25 (3), 20-21.