Related Experiment Video
Updated: Aug 11, 2026

A Package of Established Analytical Tools to Investigate the Solid-State Alteration of Lipid-Based Excipients
Published on: August 9, 2022
Assuring quality and performance of sustained and controlled release parenterals: AAPS workshop report, co-sponsored
Diane J Burgess1, Ajaz S Hussain, Thomas S Ingallinera
1Department of Pharmaceutics, University of Connecticut, 372 Fairfield Road, Storrs, Connecticut 06269, USA. dburgess@uconnvm.uconn.edu
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.
Related Concept Videos
Clinically Relevant Drug Product Specifications: Methods of Establishment
Pharmaceutical Alternatives: Polymorphic Form-Related and Particle Size-Related Therapeutic Nonequivalence
FDA Approved Drugs: Changes to Approved Drugs
Modified-Release Drug Delivery Systems: Influencing Factors
Modified-Release Drug Delivery Systems: Rate-Programmed I
Parenteral Drug Delivery Systems: Injectables, Implants, and Infusion Devices

