Assuring quality and performance of sustained and controlled release parenterals: AAPS workshop report,co-sponsored by FDA and USP |
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Authors: | Burgess Diane J Hussain Ajaz S Ingallinera Thomas S Chen Mei-Ling |
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Affiliation: | (1) Department of Pharmaceutics, University of Connecticut, 372 Fairfield Road, Storrs, Connecticut, 06269;(2) Office of Pharmaceutical Science, Center for Drug Evaluation and Research, Food and Drug Administration, 1451 Rockville Pike, HFD-350, Rockville, Maryland, 20857;(3) InfiMed Therapeutics, Inc., 8 Lantern Rd., Framingham, MA, 01702 |
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Abstract: | This is a summary report of the American Association of Pharmaceutical Scientists, the Food and Drug Administration, and the United States Pharmacopoeia cosponsored workshop on Assuring Quality and Performance of Sustained and Controlled Release Parenterals. Experts from the pharmaceutical industry, the regulatory authorities, and academia participated in this workshop to review, discuss, and debate formulation, processing, and manufacture of sustained and controlled release parenterals and identify critical process parameters and their control. Areas were identified where research is needed to understand the performance of these drug delivery systems and to assist in the development of appropriate testing procedures. Recommendations were made for future workshops, meetings, and working groups in this area. |
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